GJB2 as Well as SLC26A4 Gene Mutations are Prominent Causes for Congenital Deafness

标题
GJB2 as Well as SLC26A4 Gene Mutations are Prominent Causes for Congenital Deafness
作者
关键词
GBJ2, GBJ3, Congenital hearing loss, Mitochondrial 12S rRNA
出版物
CELL BIOCHEMISTRY AND BIOPHYSICS
Volume 73, Issue 1, Pages 41-44
出版商
Springer Nature
发表日期
2015-02-04
DOI
10.1007/s12013-015-0562-3

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