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NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss. (2021)

Abstract

No abstract provided

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