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

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: One hundr...

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Detalles Bibliográficos
Autores principales: Naddafnia, Hossein, Noormohammadi, Zahra, Irani, Shiva, Salahshoorifar, Iman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625131/
https://www.ncbi.nlm.nih.gov/pubmed/31162818
http://dx.doi.org/10.1002/mgg3.780

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625131/
https://www.ncbi.nlm.nih.gov/pubmed/31162818
http://dx.doi.org/10.1002/mgg3.780

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