A Novel Connexin 26 Mutation Associated with Autosomal Recessive Sensorineural Deafness
about
Connexin 26 mutations in autosomal recessive deafness disorders: a reviewA Mayan founder mutation is a common cause of deafness in Guatemala.Screening of genetic alterations related to non-syndromic hearing loss using MassARRAY iPLEX® technologyDFNB1 Non-syndromic Hearing Impairment: Diversity of Mutations and Associated Phenotypes.
P2860
A Novel Connexin 26 Mutation Associated with Autosomal Recessive Sensorineural Deafness
description
im Januar 2004 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 01 January 2004
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в грудні 2003
@uk
name
A Novel Connexin 26 Mutation Associated with Autosomal Recessive Sensorineural Deafness
@en
A Novel Connexin 26 Mutation Associated with Autosomal Recessive Sensorineural Deafness
@nl
type
label
A Novel Connexin 26 Mutation Associated with Autosomal Recessive Sensorineural Deafness
@en
A Novel Connexin 26 Mutation Associated with Autosomal Recessive Sensorineural Deafness
@nl
prefLabel
A Novel Connexin 26 Mutation Associated with Autosomal Recessive Sensorineural Deafness
@en
A Novel Connexin 26 Mutation Associated with Autosomal Recessive Sensorineural Deafness
@nl
P2093
P50
P356
P1476
A novel connexin 26 mutation associated with autosomal recessive sensorineural deafness
@en
P2093
Franz J Wachtler
Karin Kirschhofer
Klara Weipoltshammer
Klemens Frei
Reinhard Ramsebner
Wolf-Dieter Baumgartner
P356
10.1159/000074186
P577
2004-01-01T00:00:00Z