about
A novel KCNQ4 mutation and a private IMMP2L-DOCK4 duplication segregating with nonsyndromic hearing loss in a Brazilian familyComprehensive genetic screening of KCNQ4 in a large autosomal dominant nonsyndromic hearing loss cohort: genotype-phenotype correlations and a founder mutation.Progress and prospects in human genetic research into age-related hearing impairment.An analysis of the inheritance pattern of an adult-onset hearing loss in Border Collie dogs.The role of the cytosolic HSP70 chaperone system in diseases caused by misfolding and aberrant trafficking of ion channels
P2860
description
2012 nî lūn-bûn
@nan
2012 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Genetics of hearing loss: focus on DFNA2.
@ast
Genetics of hearing loss: focus on DFNA2.
@en
type
label
Genetics of hearing loss: focus on DFNA2.
@ast
Genetics of hearing loss: focus on DFNA2.
@en
prefLabel
Genetics of hearing loss: focus on DFNA2.
@ast
Genetics of hearing loss: focus on DFNA2.
@en
P2860
P356
P1476
Genetics of hearing loss: focus on DFNA2.
@en
P2093
Kelley M Dodson
Laura M Dominguez
P2860
P304
P356
10.2147/TACG.S35525
P577
2012-10-18T00:00:00Z