Exome Sequencing Identifies a Mutation in EYA4 as a Novel...

PLoS ONE 2015 / 5 Vol. 10; Iss. 5

Exome Sequencing Identifies a Mutation in EYA4 as a Novel Cause of Autosomal Dominant Non-Syndromic Hearing Loss

Liu, Fei, Hu, Jiongjiong, Xia, Wenjun, Hao, Lili, Ma, Jing, Ma, Duan, Ma, Zhaoxin, Alsina, Berta
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Volume:
10
Language:
english
Journal:
PLOS ONE
DOI:
10.1371/journal.pone.0126602
Date:
May, 2015
File:
PDF, 2.45 MB
english, 2015
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