The Study of SLC26A4 Gene Causing Autosomal Recessive Hearing Loss by Linkage Analysis in a Cohort of Iranian Populations

Sensorineural non-syndromic hearing loss is the most common disorder which affects 1 in 500 newborns. Hearing loss is an extremely heterogeneous defect with more than 100 loci identified to date. According to the studies, mutations in GJB2 are estimated to be involved in 50- 80% of autosomal recessi...

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Detalles Bibliográficos
Autores principales: Reiisi, Somayeh, Sanati, Mohammad Hosein, Tabatabaiefar, Mohammad Amin, Ahmadian, Shahla, Reiisi, Salimeh, Parchami, Shahrbanoo, Porjafari, Hamid, Shahi, Heshmat, Shavarzi, Afsaneh, Hashemzade Chaleshtori, Morteza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Babol University of Medical Sciences 2014
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4170491/
https://www.ncbi.nlm.nih.gov/pubmed/25317404

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4170491/
https://www.ncbi.nlm.nih.gov/pubmed/25317404

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