Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Maria Asaad"'
Publikováno v:
Human Genomics, Vol 17, Iss 1, Pp 1-10 (2023)
Abstract Background Hearing loss is a rare hereditary deficit that is rather common among consanguineous populations. Autosomal recessive non-syndromic hearing loss is the predominant form of hearing loss worldwide. Although prevalent, hearing loss i
Externí odkaz:
https://doaj.org/article/9844d87463d34aa580257b0829e3ac7c
