Zobrazeno 1 - 1
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pro vyhledávání: '"Vallian Broujeni S"'
Publikováno v:
مجله دانشگاه علوم پزشکی گرگان, Vol 16, Iss 2, Pp 82-88 (2014)
Background and Objective: SLC26A4 gene mutations after GJB2 mutations are the second currently identifiable genetic cause of autosomal recessive non syndromic hearing loss (ARNSHL) which currently is used in molecular diagnosis of ARNSHL. Several pot
Externí odkaz:
https://doaj.org/article/262125ffcb5542a4bd4b3d0987cb294c
