Mutation analysis of common deafness-causing genes among 506 patients with nonsyndromic hearing loss from Wenzhou city, China

出版年份 2019 全文链接

标题

作者

关键词

Nonsyndromic hearing loss, GJB2, SLC26A4, GJB3, mtDNA , 12SRNA

出版物

INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY

Volume 122, Issue -, Pages 185-190

出版商

Elsevier BV

发表日期

2019-04-21

DOI

10.1016/j.ijporl.2019.04.024

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