Whole Exome Sequencing Identified MCM2 as a Novel Causative Gene for Autosomal Dominant Nonsyndromic Deafness in a Chinese Family

Author:

Gao Juanjuan,Wang Qi,Dong Cheng,Chen Siqi,Qi Yu,Liu Yuhe

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference35 articles.

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4. Function and expression pattern of nonsyndromic deafness genes;N Hilgert;Current molecular medicine,2009

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