Prevalence of GJB2 (CX26) gene mutations in south Iranian patients with autosomal recessive nonsyndromic sensorineural hearing loss.

Hashemi, Seyed Basir

Prevalence of GJB2 (CX26) gene mutations in south Iranian patients with autosomal recessive nonsyndromic sensorineural hearing loss. [electronic resource] - Molecular biology reports Dec 2012 - 10481-7 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1573-4978

10.1007/s11033-012-1929-9 doi


Amino Acid Sequence
Connexin 26
Connexins--chemistry
Genes, Recessive--genetics
Genetic Predisposition to Disease
Geography
Hearing Loss, Sensorineural--epidemiology
Humans
Iran--epidemiology
Molecular Sequence Data
Mutation--genetics
Mutation Rate
Prevalence
Protein Structure, Tertiary