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Linkage study and exome sequencing identify a BDP1 mutation associated with hereditary hearing loss. (2013)

First Author: Girotto G

Attributed to: GRL - Prof Steel funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1371/journal.pone.0080323

PubMed Identifier: 24312468

Publication URI: http://europepmc.org/abstract/MED/24312468

Type: Journal Article/Review

Volume: 8

Parent Publication: PloS one

Issue: 12

ISSN: 1932-6203