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

Published 2015 View Full Article

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Title
GJB2 as Well as SLC26A4 Gene Mutations are Prominent Causes for Congenital Deafness
Authors
Keywords
GBJ2, GBJ3, Congenital hearing loss, Mitochondrial 12S rRNA
Journal
CELL BIOCHEMISTRY AND BIOPHYSICS
Volume 73, Issue 1, Pages 41-44
Publisher
Springer Nature
Online
2015-02-04
DOI
10.1007/s12013-015-0562-3
References
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