Extension of the clinical and molecular phenotype of DIAPH1-associated autosomal dominant hearing loss (DFNA1)

Neuhaus, C.; Lang-Roth, R.; Zimmermann, U.; Heller, R.; Eisenberger, T.; Weikert, M.; Markus, S.; Knipper, M.; Bolz, H. J.

dc.contributor.author	Zimmermann, Ulrike
dc.date.accessioned	2017-08-29T12:35:36Z
dc.date.available	2017-08-29T12:35:36Z
dc.date.issued	2017
dc.identifier.issn	1399-0004
dc.identifier.uri	http://hdl.handle.net/10900/77626
dc.language.iso	en	de_DE
dc.publisher	Wiley	de_DE
dc.relation.uri	http://dx.doi.org/10.1111/cge.12915	de_DE
dc.rights	info:eu-repo/semantics/closedAccess
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Extension of the clinical and molecular phenotype of DIAPH1-associated autosomal dominant hearing loss (DFNA1)	de_DE
dc.type	Article	de_DE
utue.quellen.id	20170815222223_00644
utue.publikation.seiten	892-901	de_DE
utue.personen.roh	Neuhaus, C.
utue.personen.roh	Lang-Roth, R.
utue.personen.roh	Zimmermann, U.
utue.personen.roh	Heller, R.
utue.personen.roh	Eisenberger, T.
utue.personen.roh	Weikert, M.
utue.personen.roh	Markus, S.
utue.personen.roh	Knipper, M.
utue.personen.roh	Bolz, H. J.
dcterms.isPartOf.ZSTitelID	Clinical Genetics	de_DE
dcterms.isPartOf.ZS-Issue	6	de_DE
dcterms.isPartOf.ZS-Volume	91	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE