Hearing impairment in genotyped Wolfram syndrome patients.
about
Genetics of hearing and deafnessAudiologic and vestibular findings in Wolfram syndromeAutosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1Diabetes mellitus, diabetes insipidus, optic atrophy, and deafness: A case of Wolfram (DIDMOAD) syndromeWolfram syndrome and WFS1 gene.Genetics of non syndromic hearing loss.Wolfram syndrome: a clinicopathologic correlation.A clinical case study of a Wolfram syndrome-affected family: pattern-reversal visual evoked potentials and electroretinography analysis.Presentation and clinical course of Wolfram (DIDMOAD) syndrome from North India.A novel mutation of WFS1 gene in a Chinese patient with Wolfram syndrome: a case report.Longitudinal hearing loss in Wolfram syndrome.
P2860
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P2860
Hearing impairment in genotyped Wolfram syndrome patients.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
Hearing impairment in genotyped Wolfram syndrome patients.
@en
Hearing impairment in genotyped Wolfram syndrome patients.
@nl
type
label
Hearing impairment in genotyped Wolfram syndrome patients.
@en
Hearing impairment in genotyped Wolfram syndrome patients.
@nl
prefLabel
Hearing impairment in genotyped Wolfram syndrome patients.
@en
Hearing impairment in genotyped Wolfram syndrome patients.
@nl
P2093
P2860
P1476
Hearing impairment in genotyped Wolfram syndrome patients.
@en
P2093
Bernard Vialettes
Cor W R J Cremers
Fortunato Lombardo
Patrick L M Huygen
Philipp Eller
Ronald J E Pennings
Rutger F Plantinga
Veronique Paquis-Fluklinger
P2860
P304
P356
10.1177/000348940811700704
P577
2008-07-01T00:00:00Z