Investigation of LRTOMT gene (locus DFNB63) mutations in Iranian patients with autosomal recessive non-syndromic hearing loss

Hearing loss (HL) is the most frequent sensory defect affecting 1 in 1000 neonates. This can occur due to genetic or environmental causes or both. The genetic causes are very heterogenous and over 100 loci have been identified to cause autosomal recessive non - syndromic hearing loss (ARNSHL). The a...

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Detalles Bibliográficos
Autores principales: Taghizadeh, Seyyed Hossein, Kazeminezhad, Seyyed Reza, Sefidgar, Seyyed Ali Asghar, Yazdanpanahi, Nasrin, Tabatabaeifar, Mohammad Amin, Yousefi, Ahmad, Lesani, Seyyed Mohammad, Abolhasani, Marziyeh, Hashemzadeh Chaleshtori, Morteza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Babol University of Medical Sciences 2013
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3920523/
https://www.ncbi.nlm.nih.gov/pubmed/24551789

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