Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing loss
about
Is TMC1 the Hair Cell Mechanotransducer Channel?Utilization of amplicon-based targeted sequencing panel for the massively parallel sequencing of sporadic hearing impairment patients from Saudi ArabiaIdentification of Pathogenic Genes of Nonsyndromic Hearing Loss in Uyghur Families Using Massively Parallel DNA Sequencing Technique.Identification of four TMC1 variations in different Chinese families with hereditary hearing loss.Mutation spectra and founder effect of TMC1 in patients with non-syndromic deafness in Xiamen area, China.
P2860
Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing loss
description
2016 nî lūn-bûn
@nan
2016 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
Exome sequencing identifies a ...... sive nonsyndromic hearing loss
@ast
Exome sequencing identifies a ...... sive nonsyndromic hearing loss
@en
Exome sequencing identifies a ...... sive nonsyndromic hearing loss
@nl
type
label
Exome sequencing identifies a ...... sive nonsyndromic hearing loss
@ast
Exome sequencing identifies a ...... sive nonsyndromic hearing loss
@en
Exome sequencing identifies a ...... sive nonsyndromic hearing loss
@nl
prefLabel
Exome sequencing identifies a ...... sive nonsyndromic hearing loss
@ast
Exome sequencing identifies a ...... sive nonsyndromic hearing loss
@en
Exome sequencing identifies a ...... sive nonsyndromic hearing loss
@nl
P2093
P2860
P3181
P1476
Exome sequencing identifies a ...... sive nonsyndromic hearing loss
@en
P2093
Jiongjiong Hu
Wenjun Xia
Zhaoxin Ma
Zhenghua Zhu
P2860
P2888
P3181
P356
10.1186/S12967-016-0780-5
P577
2016-01-28T00:00:00Z
P6179
1020212325