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Phosphatidylinositol 4-kinase β mutations cause nonsyndromic sensorineural deafness and inner ear ma
[期刊论文] 作者：Shuilong Wu,Guoan Li,Franz Rüschendorf,Lei Zhao,Hongwei Cui,Junqing Liang,Liang Fang,Hao Hu,Sebastian Froehler,
来源：遗传学报 年份：2020
Congenital hearing loss is a common disorder worldwide.Heterogeneous gene variation accounts for approximately 20-25％of such patients.We investigated a five-gene...
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