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pro vyhledávání: '"Shin-Ya Nisio"'
Autor:
Yasuhiro Arai, Masahiro Takahashi, Naoko Sakuma, Shin-Ya Nisio, Nobuhiko Oridate, Shin-Ichi Usami
Publikováno v:
Acta Oto-Laryngologica Case Reports, Vol 2, Iss 1, Pp 137-140 (2017)
GJB2 gene mutation is the most common cause of congenital sensorineural hearing loss worldwide. Most GJB2 gene mutations have been associated with autosomal recessive non-syndromic hearing loss (DFNB1), but some are also associated with autosomal dom
Externí odkaz:
https://doaj.org/article/cdf9bb0ce1e145bebd692cfe0dd24350