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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Babol University of Medical Sciences 2013
Assuntos:
Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3920523/
https://ncbi.nlm.nih.gov/pubmed/24551789
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados