MYH1 is a candidate gene for recurrent rhabdomyolysis in humans-Reference-Cited by-同舟云学术

MYH1 is a candidate gene for recurrent rhabdomyolysis in humans

Published:2021-03-23 Issue:7 Volume:185 Page:2131-2135
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Alsaif Hessa S.¹^ORCID,Alshehri Ali²,Sulaiman Raashda A.³^ORCID,Al‐Hindi Hindi⁴,Guzmán‐Vega Francisco J.⁵,Arold Stefan T.⁵⁶,Alkuraya Fowzan S.¹⁷^ORCID

Affiliation:

1. Department of Translational Genomics, Center for Genomic Medicine King Faisal Specialist Hospital and Research Center Riyadh Saudi Arabia

2. Department of Neuroscience King Faisal Specialist Hospital and Research Center Riyadh Saudi Arabia

3. Department of Medical Genetics King Faisal Specialist Hospital and Research Center Riyadh Saudi Arabia

4. Department of Pathology and Laboratory Medicine King Faisal Specialist Hospital and Research Center Riyadh Saudi Arabia

5. King Abdullah University of Science and Technology (KAUST), Computational Bioscience Research Center (CBRC) Division of Biological and Environmental Sciences and Engineering (BESE) Thuwal Saudi Arabia

6. Centre de Biochimie Structurale CNRS, INSERM, Université de Montpellier Montpellier France

7. Department of Anatomy and Cell Biology College of Medicine Riyadh Saudi Arabia

Funder

King Abdullah University of Science and Technology

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62188

Reference15 articles.

1. A syndrome of congenital hyperinsulinism and rhabdomyolysis is caused byKCNJ11mutation