Vestibular function in families with inherited autosomal dominant hearing loss.

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P2860

Q30412991-99F68141-2F51-4927-BBCA-C00D91708DDE Q55004054-70E47E86-2284-4AD6-95AC-64F4379B4F89

P2860

Vestibular function in families with inherited autosomal dominant hearing loss.

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http://www.wikidata.org/entity/Q36955586

description

2008 nî lūn-bûn

@nan

2008年の論文

@ja

2008年論文

@yue

2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

@zh-mo

2008年論文

@zh-tw

2008年论文

@wuu

2008年论文

@zh

2008年论文

@zh-cn

name

Vestibular function in families with inherited autosomal dominant hearing loss.

@en

type

Item

label

Vestibular function in families with inherited autosomal dominant hearing loss.

@en

prefLabel

Vestibular function in families with inherited autosomal dominant hearing loss.

@en

P1476

Vestibular function in families with inherited autosomal dominant hearing loss.

@en

P2093

James O Phillips

http://www.w3.org/2001/XMLSchema#string

Jeremy C Kallman

http://www.w3.org/2001/XMLSchema#string

Naomi F Bramhall

http://www.w3.org/2001/XMLSchema#string

Paul D Strombom

http://www.w3.org/2001/XMLSchema#string

Valerie A Street

http://www.w3.org/2001/XMLSchema#string

P2860

Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11)

Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues.

Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4)

A novel TECTA mutation in a Dutch DFNA8/12 family confirms genotype-phenotype correlation

Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation

Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease

A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects

Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11).

Autosomal dominant non-syndromal low-frequency sensorineural hearing impairment linked to chromosome 4p16 (DFNA14): statistical analysis of hearing threshold in relation to age and evaluation of vestibulo-ocular functions.

Association of clinical features with mutation of TECTA in a family with autosomal dominant hearing loss.

P304

51-58

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P31

scholarly article

review article

P433

http://www.w3.org/2001/XMLSchema#string

P478

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P577

2008-01-01T00:00:00Z

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P698

18776598

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P932

2575737

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Vestibular function in families with inherited autosomal dominant hearing loss.

about

P2860

P2860

Vestibular function in families with inherited autosomal dominant hearing loss.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P433

P478

P577

P698

P932

P1433

P1476

P2093

P2860

P304

P31

P433

P478

P577

P698

P932