Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis. (2012)
Attributed to:
Identification of copy number variants in familial and pathologically proven PD
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2012.10.024
PubMed Identifier: 23200863
Publication URI: http://europepmc.org/abstract/MED/23200863
Type: Journal Article/Review
Volume: 91
Parent Publication: American journal of human genetics
Issue: 6
ISSN: 0002-9297