NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss. (2021)
Abstract
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Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddaa240
PubMed Identifier: 33326993
Publication URI: http://europepmc.org/abstract/MED/33326993
Type: Journal Article/Review
Volume: 29
Parent Publication: Human molecular genetics
Issue: 22
ISSN: 0964-6906