Phenotype analysis of an Australian DFNA9 family with the 1109N COCH mutation.
about
Different Phenotypes of the Two Chinese Probands with the Same c.889G>A (p.C162Y) Mutation in COCH Gene Verify Different Mechanisms Underlying Autosomal Dominant Nonsyndromic Deafness 9.Progress and prospects in human genetic research into age-related hearing impairment.Does Otovestibular Loss in the Autosomal Dominant Disorder DFNA9 Have an Impact of on Cognition? A Systematic Review.
P2860
Phenotype analysis of an Australian DFNA9 family with the 1109N COCH mutation.
description
2011 nî lūn-bûn
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2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
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2011年學術文章
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name
Phenotype analysis of an Australian DFNA9 family with the 1109N COCH mutation.
@en
Phenotype analysis of an Australian DFNA9 family with the 1109N COCH mutation.
@nl
type
label
Phenotype analysis of an Australian DFNA9 family with the 1109N COCH mutation.
@en
Phenotype analysis of an Australian DFNA9 family with the 1109N COCH mutation.
@nl
prefLabel
Phenotype analysis of an Australian DFNA9 family with the 1109N COCH mutation.
@en
Phenotype analysis of an Australian DFNA9 family with the 1109N COCH mutation.
@nl
P2093
P2860
P1476
Phenotype analysis of an Australian DFNA9 family with the 1109N COCH mutation.
@en
P2093
Cor W R J Cremers
Gordon M Colditz
Patrick L M Huygen
Robert J Pauw
P2860
P304
P356
10.1177/000348941112000612
P577
2011-06-01T00:00:00Z