OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67). (2015)

First Author: Thoenes M

Attributed to: GRL - Prof Steel funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1186/s13023-015-0238-5

PubMed Identifier: 25759012

Publication URI: http://europepmc.org/abstract/MED/25759012

Type: Journal Article/Review

Volume: 10

Parent Publication: Orphanet journal of rare diseases

ISSN: 1750-1172