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