Mutation Screening of Exons 7 and 13 of the TMC1 Gene in Autosomal Recessive Non-syndromic Hearing Loss (ARNSHL) in Iran

BACKGROUND: Non-syndromic hearing loss (NSHL) is the most common birth defect and occurs in approximately 1/1,000 newborns. NSHL is a heterogeneous trait and can arise due to both genetic and environmental factors. Mutations of the transmembrane channel-like 1 (TMC1) gene cause non-syndromic deafnes...

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Detalles Bibliográficos
Autores principales: Moradipour, Negar, Ghasemi-Dehkordi, Payam, Heibati, Fatemeh, Parchami-Barjui, Shahrbanuo, Abolhasani, Marziyeh, Rashki, Ahmad, Hashemzadeh-Chaleshtori, Morteza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4884626/
https://www.ncbi.nlm.nih.gov/pubmed/27247785
http://dx.doi.org/10.5812/ircmj.22076

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4884626/
https://www.ncbi.nlm.nih.gov/pubmed/27247785
http://dx.doi.org/10.5812/ircmj.22076

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