The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?
about
Identification of pathogenic mechanisms of COCH mutations, abolished cochlin secretion, and intracellular aggregate formation: genotype-phenotype correlations in DFNA9 deafness and vestibular disorder.The genetic bases for non-syndromic hearing loss among ChineseGene expression profiles of the cochlea and vestibular endorgans: localization and function of genes causing deafness.Finnish familial Meniere disease is not linked to chromosome 12p12.3, and anticipation and cosegregation with migraine are not common findings.
P2860
The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh-hant
name
The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?
@en
The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?
@nl
type
label
The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?
@en
The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?
@nl
prefLabel
The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?
@en
The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?
@nl
P2860
P1476
The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?
@en
P2093
P2860
P304
P356
10.3109/03005369909090113
P577
1999-10-01T00:00:00Z