Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features

doi:10.1007/s00439-017-1828-1

Published Erratum

. 2017 Aug;136(8):1009-1011.

doi: 10.1007/s00439-017-1828-1.

Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features

Jing Zhang^{1

2}, Tomasz Gambin^{1

3

4}, Bo Yuan^{1

2}, Przemyslaw Szafranski¹, Jill A Rosenfeld¹, Mohammed Al Balwi⁵, Abdulrahman Alswaid⁶, Lihadh Al-Gazali⁷, Aisha M Al Shamsi⁸, Makanko Komara⁹, Bassam R Ali⁹, Elizabeth Roeder^{1

10}, Laura McAuley¹¹, Daniel S Roy¹², David K Manchester¹³, Pilar Magoulas¹, Lauren E King¹⁴, Vickie Hannig¹⁴, Dominique Bonneau^{15

16}, Anne-Sophie Denommé-Pichon^{15

16}, Majida Charif¹⁶, Thomas Besnard¹⁷, Stéphane Bézieau¹⁷, Benjamin Cogné¹⁷, Joris Andrieux¹⁸, Wenmiao Zhu^{1

2}, Weimin He^{1

2}, Francesco Vetrini^{1

2}, Patricia A Ward^{1

2}, Sau Wai Cheung^{1

2}, Weimin Bi^{1

2}, Christine M Eng^{1

2}, James R Lupski^{1

19

20

21}, Yaping Yang^{1

2}, Ankita Patel^{1

2}, Seema R Lalani^{1

2}, Fan Xia^{22

23}, Paweł Stankiewicz^{24

25}

Affiliations

¹ Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, TX, 77030, USA.
² Baylor Genetics, Houston, TX, 77021, USA.
³ Institute of Computer Science, Warsaw University of Technology, Warsaw, 02-038, Poland.
⁴ Department of Medical Genetics, Institute of Mother and Child, Warsaw, 01-211, Poland.
⁵ Pathology and Laboratory Medicine, King Abdulaziz Medical City, Riyadh, 11246, Saudi Arabia.
⁶ Department of Pediatrics, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
⁷ Department of Pediatrics, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates.
⁸ Department of Pediatrics, Tawam Hospital, Al Ain, United Arab Emirates.
⁹ Department of Pathology, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates.
¹⁰ Departments of Pediatrics and Molecular and Human Genetics, Baylor College of Medicine, San Antonio, TX, 78230, USA.
¹¹ UT Southwestern Medical Center, Children's Health Children's Medical Center, Dallas, TX, 75235, USA.
¹² Tripler Army Medical Center, Honolulu, 96859, USA.
¹³ Genetics and Metabolism, Children's Hospital, Aurora, CO, 80045, USA.
¹⁴ Vanderbilt Children's Hospital, Nashville, TN, 37232, USA.
¹⁵ Department of Biochemistry and Genetics, University Hospital, 49933, Angers Cedex 9, France.
¹⁶ UMR CNRS 6015-INSERM 1083 and PREMMI, University of Angers, 49933, Angers Cedex 9, France.
¹⁷ CHU Nantes, Service de Génétique Médicale, 9 quai Moncousu, 44093, Nantes Cedex 1, France.
¹⁸ Institute of Medical Genetics, Jeanne de Flandre Hospital, Lille University Hospital, Lille, 59800, France.
¹⁹ Department of Pediatrics, Baylor College of Medicine, Houston, TX, 77030, USA.
²⁰ Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, 77030, USA.
²¹ Texas Children's Hospital, Houston, TX, 77030, USA.
²² Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, TX, 77030, USA. fxia@bcm.edu.
²³ Baylor Genetics, Houston, TX, 77021, USA. fxia@bcm.edu.
²⁴ Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, TX, 77030, USA. pawels@bcm.edu.
²⁵ Baylor Genetics, Houston, TX, 77021, USA. pawels@bcm.edu.

PMID: 28660352
DOI: 10.1007/s00439-017-1828-1

Published Erratum

Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features

Jing Zhang et al. Hum Genet. 2017 Aug.

. 2017 Aug;136(8):1009-1011.

doi: 10.1007/s00439-017-1828-1.

Authors

Affiliations

¹ Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, TX, 77030, USA.
² Baylor Genetics, Houston, TX, 77021, USA.
³ Institute of Computer Science, Warsaw University of Technology, Warsaw, 02-038, Poland.
⁴ Department of Medical Genetics, Institute of Mother and Child, Warsaw, 01-211, Poland.
⁵ Pathology and Laboratory Medicine, King Abdulaziz Medical City, Riyadh, 11246, Saudi Arabia.
⁶ Department of Pediatrics, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
⁷ Department of Pediatrics, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates.
⁸ Department of Pediatrics, Tawam Hospital, Al Ain, United Arab Emirates.
⁹ Department of Pathology, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates.
¹⁰ Departments of Pediatrics and Molecular and Human Genetics, Baylor College of Medicine, San Antonio, TX, 78230, USA.
¹¹ UT Southwestern Medical Center, Children's Health Children's Medical Center, Dallas, TX, 75235, USA.
¹² Tripler Army Medical Center, Honolulu, 96859, USA.
¹³ Genetics and Metabolism, Children's Hospital, Aurora, CO, 80045, USA.
¹⁴ Vanderbilt Children's Hospital, Nashville, TN, 37232, USA.
¹⁵ Department of Biochemistry and Genetics, University Hospital, 49933, Angers Cedex 9, France.
¹⁶ UMR CNRS 6015-INSERM 1083 and PREMMI, University of Angers, 49933, Angers Cedex 9, France.
¹⁷ CHU Nantes, Service de Génétique Médicale, 9 quai Moncousu, 44093, Nantes Cedex 1, France.
¹⁸ Institute of Medical Genetics, Jeanne de Flandre Hospital, Lille University Hospital, Lille, 59800, France.
¹⁹ Department of Pediatrics, Baylor College of Medicine, Houston, TX, 77030, USA.
²⁰ Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, 77030, USA.
²¹ Texas Children's Hospital, Houston, TX, 77030, USA.
²² Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, TX, 77030, USA. fxia@bcm.edu.
²³ Baylor Genetics, Houston, TX, 77021, USA. fxia@bcm.edu.
²⁴ Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, TX, 77030, USA. pawels@bcm.edu.
²⁵ Baylor Genetics, Houston, TX, 77021, USA. pawels@bcm.edu.

PMID: 28660352
DOI: 10.1007/s00439-017-1828-1

No abstract available

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Erratum for

Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features.
Zhang J, Gambin T, Yuan B, Szafranski P, Rosenfeld JA, Balwi MA, Alswaid A, Al-Gazali L, Shamsi AMA, Komara M, Ali BR, Roeder E, McAuley L, Roy DS, Manchester DK, Magoulas P, King LE, Hannig V, Bonneau D, Denommé-Pichon AS, Charif M, Besnard T, Bézieau S, Cogné B, Andrieux J, Zhu W, He W, Vetrini F, Ward PA, Cheung SW, Bi W, Eng CM, Lupski JR, Yang Y, Patel A, Lalani SR, Xia F, Stankiewicz P. Zhang J, et al. Hum Genet. 2017 Apr;136(4):377-386. doi: 10.1007/s00439-017-1763-1. Epub 2017 Mar 1. Hum Genet. 2017. PMID: 28251352 Free PMC article.

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van der Laan L, Rooney K, Alders M, Relator R, McConkey H, Kerkhof J, Levy MA, Lauffer P, Aerden M, Theunis M, Legius E, Tedder ML, Vissers LELM, Koene S, Ruivenkamp C, Hoffer MJV, Wieczorek D, Bramswig NC, Herget T, González VL, Santos-Simarro F, Tørring PM, Denomme-Pichon AS, Isidor B, Keren B, Julia S, Schaefer E, Francannet C, Maillard PY, Misra-Isrie M, Van Esch H, Mannens MMAM, Sadikovic B, van Haelst MM, Henneman P. van der Laan L, et al. Int J Mol Sci. 2022 Nov 8;23(22):13664. doi: 10.3390/ijms232213664. Int J Mol Sci. 2022. PMID: 36430143 Free PMC article.
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Dong X, Liu B, Yang L, Wang H, Wu B, Liu R, Chen H, Chen X, Yu S, Chen B, Wang S, Xu X, Zhou W, Lu Y. Dong X, et al. J Med Genet. 2020 Aug;57(8):558-566. doi: 10.1136/jmedgenet-2019-106377. Epub 2020 Jan 31. J Med Genet. 2020. PMID: 32005694 Free PMC article.
Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder.
Frints SGM, Ozanturk A, Rodríguez Criado G, Grasshoff U, de Hoon B, Field M, Manouvrier-Hanu S, E Hickey S, Kammoun M, Gripp KW, Bauer C, Schroeder C, Toutain A, Mihalic Mosher T, Kelly BJ, White P, Dufke A, Rentmeester E, Moon S, Koboldt DC, van Roozendaal KEP, Hu H, Haas SA, Ropers HH, Murray L, Haan E, Shaw M, Carroll R, Friend K, Liebelt J, Hobson L, De Rademaeker M, Geraedts J, Fryns JP, Vermeesch J, Raynaud M, Riess O, Gribnau J, Katsanis N, Devriendt K, Bauer P, Gecz J, Golzio C, Gontan C, Kalscheuer VM. Frints SGM, et al. Mol Psychiatry. 2019 Nov;24(11):1748-1768. doi: 10.1038/s41380-018-0065-x. Epub 2018 May 4. Mol Psychiatry. 2019. PMID: 29728705

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Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features

Affiliations

Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features

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