A novel missense variant in MYO3A is associated with autosomal dominant high-frequency hearing loss in a German family

Doll, Julia; Hofrichter, Michaela A. H.; Bahena, Paulina; Heihoff, Alfred; Segebarth, Dennis; Mueller, Tobias; Dittrich, Marcus; Haaf, Thomas; Vona, Barbara

dc.contributor.author	Vona, Barbara
dc.date.accessioned	2020-08-31T08:29:39Z
dc.date.available	2020-08-31T08:29:39Z
dc.date.issued	2020
dc.identifier.issn	2324-9269
dc.identifier.uri	http://hdl.handle.net/10900/105910
dc.language.iso	en	de_DE
dc.publisher	Wiley	de_DE
dc.relation.uri	http://dx.doi.org/10.1002/mgg3.1343	de_DE
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	A novel missense variant in MYO3A is associated with autosomal dominant high-frequency hearing loss in a German family	de_DE
dc.type	Article	de_DE
utue.quellen.id	20200715072417_00185
utue.personen.roh	Doll, Julia
utue.personen.roh	Hofrichter, Michaela A. H.
utue.personen.roh	Bahena, Paulina
utue.personen.roh	Heihoff, Alfred
utue.personen.roh	Segebarth, Dennis
utue.personen.roh	Mueller, Tobias
utue.personen.roh	Dittrich, Marcus
utue.personen.roh	Haaf, Thomas
utue.personen.roh	Vona, Barbara
dcterms.isPartOf.ZSTitelID	Molecular Genetics & Genomic Medicine	de_DE
dcterms.isPartOf.ZS-Issue	Article e1343	de_DE
dcterms.isPartOf.ZS-Volume	8	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE