Extralabyrinthine manifestations of DFNA9 - Test2 - elhamkhani - TriplyDB

Extralabyrinthine manifestations of DFNA9

Extralabyrinthine manifestations of DFNA9

http://www.wikidata.org/entity/Q34612963

about

Cochlin in normal middle ear and abnormal middle ear deposits in DFNA9 and Coch (G88E/G88E) mice.Histopathology of the Human Inner Ear in the p.L114P COCH Mutation (DFNA9).Immunohistochemical techniques for the human inner ear.Does Otovestibular Loss in the Autosomal Dominant Disorder DFNA9 Have an Impact of on Cognition? A Systematic Review.

P2860

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P2860

Extralabyrinthine manifestations of DFNA9

http://www.wikidata.org/entity/Q34612963

description

2010 nî lūn-bûn

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2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Extralabyrinthine manifestations of DFNA9

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Extralabyrinthine manifestations of DFNA9

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Extralabyrinthine manifestations of DFNA9

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type

label

Extralabyrinthine manifestations of DFNA9

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Extralabyrinthine manifestations of DFNA9

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Extralabyrinthine manifestations of DFNA9

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prefLabel

Extralabyrinthine manifestations of DFNA9

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Extralabyrinthine manifestations of DFNA9

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Extralabyrinthine manifestations of DFNA9

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Extralabyrinthine manifestations of DFNA9

@en

P2093

Andrew A McCall

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

Fred H Linthicum

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

Jennifer T O'Malley

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

Joe C Adams

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

Jose N Fayad

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

Marc K Bassim

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

Robert Gellibolian

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

Saumil N Merchant

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

P2860

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction

Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4

A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13

Autosomal dominant sensorineural hearing loss. Pedigrees, audiologic findings, and temporal bone findings in two kindreds

Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening

Preoperative predictors of incudal necrosis in chronic suppurative otitis media.

Anatomy of the distal incus in humans.

A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction

Vestibular deterioration precedes hearing deterioration in the P51S COCH mutation (DFNA9): an analysis in 74 mutation carriers.

Role of protein misfolding in DFNA9 hearing loss.

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141-149

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scholarly article

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10.1007/S10162-010-0245-0

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2

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