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

DSpace Repository

Show simple item record

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 Artikel 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


Files in this item

Files Size Format View

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record