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A novel connexin 26 mutation associated with autosomal recessive sensorineural deafness

dc.contributor.authorWeipoltshammer, Klara
dc.contributor.authorErginel-Unaltuna, Nihan
dc.contributor.authorBaumgartner, Wolf-Dieter
dc.contributor.authorWachtler, Franz J.
dc.contributor.authorKirschhofer, Karin
dc.contributor.authorFrei, Klemens
dc.contributor.authorLucas, Trevor
dc.contributor.authorRamsebner, Reinhard
dc.contributor.authorSchöfer, Christian
dc.date.accessioned2021-03-05T14:40:20Z
dc.date.available2021-03-05T14:40:20Z
dc.date.issued2004
dc.identifier.citationFrei K., Lucas T., Ramsebner R., Schöfer C., Baumgartner W., Weipoltshammer K., Erginel-Unaltuna N., Wachtler F. J. , Kirschhofer K., "A novel connexin 26 mutation associated with autosomal recessive sensorineural deafness", Audiology and Neuro-Otology, cilt.9, sa.1, ss.47-50, 2004
dc.identifier.issn1420-3030
dc.identifier.othervv_1032021
dc.identifier.otherav_b843f3bb-1048-458d-bbdc-708ec300d7e4
dc.identifier.urihttp://hdl.handle.net/20.500.12627/122614
dc.identifier.urihttps://doi.org/10.1159/000074186
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0348010573&origin=inward
dc.language.isoeng
dc.titleA novel connexin 26 mutation associated with autosomal recessive sensorineural deafness
dc.typeMakale
dc.relation.journalAudiology and Neuro-Otology
dc.contributor.departmentAllgemeines KrankenHaus Wien , ,
dc.identifier.volume9
dc.identifier.issue1
dc.identifier.startpage47
dc.identifier.endpage50
dc.contributor.firstauthorID106877


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