Prevalence of GJB2 (CX26) gene mutations in south Iranian patients with autosomal recessive nonsyndromic sensorineural hearing loss.
about
Analysis of trafficking, stability and function of human connexin 26 gap junction channels with deafness-causing mutations in the fourth transmembrane helixGJB2 c.-23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss.Analysis of common deafness gene mutations in deaf people from unique ethnic groups in Gansu Province, China.
P2860
Prevalence of GJB2 (CX26) gene mutations in south Iranian patients with autosomal recessive nonsyndromic sensorineural hearing loss.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh-hant
name
Prevalence of GJB2 (CX26) gene ...... ic sensorineural hearing loss.
@en
type
label
Prevalence of GJB2 (CX26) gene ...... ic sensorineural hearing loss.
@en
prefLabel
Prevalence of GJB2 (CX26) gene ...... ic sensorineural hearing loss.
@en
P2093
P2860
P1476
Prevalence of GJB2 (CX26) gene ...... ic sensorineural hearing loss.
@en
P2093
Masumeh Darai
Mohamad Javad Ashraf
Mohamad Saboori
Seyed Basir Hashemi
P2860
P2888
P304
10481-10487
P356
10.1007/S11033-012-1929-9
P577
2012-10-17T00:00:00Z