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Frequency of GJB2 mutations, GJB6‐D13S1830 and GJB6‐D13S1854 deletions among patients with non‐syndromic hearing loss from the central region of Iran

Abstract Background In the present study, we investigate the prevalence of the GJB2 gene mutations, and deletions in the GJB6 gene, namely del (GJB6‐D13S1830) and del (GJB6‐D13S1854), in patients with autosomal recessive non‐syndromic hearing loss (ARNSHL) from the central region of Iran. Methods On...

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Hlavní autoři: Hossein Naddafnia, Zahra Noormohammadi, Shiva Irani, Iman Salahshoorifar
Médium: Artigo
Jazyk:Inglês
Vydáno: Wiley 2019-07-01
Edice:Molecular Genetics & Genomic Medicine
Témata:
autosomal recessive nonsyndromic hearing loss
connexin 26
connexin 30
GJB2 mutation
GJB6 mutation
On-line přístup:https://doi.org/10.1002/mgg3.780
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