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

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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


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