Whole Exome Sequencing Identified MCM2 as a Novel Causative...

PLoS ONE 2015 / 7 Vol. 10; Iss. 7

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

Gao, Juanjuan, Wang, Qi, Dong, Cheng, Chen, Siqi, Qi, Yu, Liu, Yuhe, Bandapalli, Obul Reddy
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Volume:
10
Language:
english
Journal:
PLOS ONE
DOI:
10.1371/journal.pone.0133522
Date:
July, 2015
File:
PDF, 4.33 MB
english, 2015
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