Novel Compound Heterozygous Mutations in MYO7A Associated with Usher Syndrome 1 in a Chinese Family

Usher syndrome is an autosomal recessive disease characterized by sensorineural hearing loss, age-dependent retinitis pigmentosa (RP), and occasionally vestibular dysfunction. The most severe form is Usher syndrome type 1 (USH1). Mutations in the MYO7A gene are responsible for USH1 and account for 2...

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Detalles Bibliográficos
Autores principales: Gao, Xue, Wang, Guo-Jian, Yuan, Yong-Yi, Xin, Feng, Han, Ming-Yu, Lu, Jing-Qiao, Zhao, Hui, Yu, Fei, Xu, Jin-Cao, Zhang, Mei-Guang, Dong, Jiang, Lin, Xi, Dai, Pu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4117490/
https://www.ncbi.nlm.nih.gov/pubmed/25080338
http://dx.doi.org/10.1371/journal.pone.0103415

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4117490/
https://www.ncbi.nlm.nih.gov/pubmed/25080338
http://dx.doi.org/10.1371/journal.pone.0103415

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