GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran

OBJECTIVE: Autosomal‐recessive nonsyndromic hearing loss (ARNSHL) is a heterogeneous genetic disorder. Mutations in the gap junction protein beta 2 (GJB2) gene, encoding connexin 26, are a significant cause of ARNSHL in different ethnic groups. This study aimed to identify the frequency and type of...

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Detalles Bibliográficos
Autores principales: Abbaspour Rodbaneh, Ehsan, Panahi, Mohammad, Rahimi, Bahareh, Mokabber, Haleh, Farajollahi, Reza, Davarnia, Behzad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8605150/
https://www.ncbi.nlm.nih.gov/pubmed/34581455
http://dx.doi.org/10.1002/jcla.24024

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8605150/
https://www.ncbi.nlm.nih.gov/pubmed/34581455
http://dx.doi.org/10.1002/jcla.24024

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