Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss

Autosomal recessive nonsyndromic hearing loss (ARNSHL) is a genetically heterogeneous sensorineural disorder, generally manifested with prelingual hearing loss and absence of other clinical manifestations. The aim of this study is to identify the pathogenic gene in a four-generation consanguineous C...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:PLoS One
Hlavní autoři: Xia, Hong, Huang, Xiangjun, Guo, Yi, Hu, Pengzhi, He, Guangxiang, Deng, Xiong, Xu, Hongbo, Yang, Zhijian, Deng, Hao
Médium: Artigo
Jazyk:Inglês
Vydáno: Public Library of Science 2015
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4550393/
https://ncbi.nlm.nih.gov/pubmed/26308726
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0136306
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky