The Study of SLC26A4 Gene Causing Autosomal Recessive Hearing Loss by Linkage Analysis in a Cohort of Iranian Populations.
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Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked familyGenetic Linkage Analysis of DFNB4, DFNB28, DFNB93 Loci in Autosomal Recessive Non-syndromic Hearing Loss: Evidence for Digenic Inheritance in GJB2 and GJB3 Mutations.
P2860
The Study of SLC26A4 Gene Causing Autosomal Recessive Hearing Loss by Linkage Analysis in a Cohort of Iranian Populations.
description
2014 nî lūn-bûn
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2014 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2014年の論文
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2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
The Study of SLC26A4 Gene Caus ...... Cohort of Iranian Populations.
@ast
The Study of SLC26A4 Gene Caus ...... Cohort of Iranian Populations.
@en
The Study of SLC26A4 Gene Caus ...... Cohort of Iranian Populations.
@nl
type
label
The Study of SLC26A4 Gene Caus ...... Cohort of Iranian Populations.
@ast
The Study of SLC26A4 Gene Caus ...... Cohort of Iranian Populations.
@en
The Study of SLC26A4 Gene Caus ...... Cohort of Iranian Populations.
@nl
prefLabel
The Study of SLC26A4 Gene Caus ...... Cohort of Iranian Populations.
@ast
The Study of SLC26A4 Gene Caus ...... Cohort of Iranian Populations.
@en
The Study of SLC26A4 Gene Caus ...... Cohort of Iranian Populations.
@nl
P2093
P2860
P1476
The Study of SLC26A4 Gene Caus ...... Cohort of Iranian Populations.
@en
P2093
Afsaneh Shavarzi
Hamid Porjafari
Heshmat Shahi
Mohammad Amin Tabatabaiefar
Mohammad Hosein Sanati
Morteza Hashemzade Chaleshtori
Salimeh Reiisi
Shahla Ahmadian
Shahrbanoo Parchami
Somayeh Reiisi
P2860
P304
P577
2014-01-01T00:00:00Z