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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Hauptverfasser: 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
Format: Artigo
Sprache:Inglês
Veröffentlicht: Babol University of Medical Sciences 2013
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Original Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3920523/
https://ncbi.nlm.nih.gov/pubmed/24551789
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