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Exome Sequencing Identifies a Novel Frameshift Mutation of MYO6 as the Cause of Autosomal Domin
ISSN号:0003-4800
期刊名称:Annals of Human Genetics
时间:2014.9.17
页码:-
相关项目:新致聋基因的鉴定及其致聋机制研究
作者:
Sham, Pak C.|Zhang, Michael Q.|Zhang, Xuegong|Yuan, Huijun|
同期刊论文项目
新致聋基因的鉴定及其致聋机制研究
期刊论文 25
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Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing loss
常染色体显性遗传性聋家系遗传学特征及外显子组测序分析
Identification of two novel missense WFS1 mutations, H696Y and R703H, in patients with non-syndromic low-frequency sensorineural hearing loss