A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia. (2015)
Attributed to:
ERANET 1 NEURON 3: 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.2015.04.008
PubMed Identifier: 25983243
Publication URI: http://europepmc.org/abstract/MED/25983243
Type: Journal Article/Review
Volume: 96
Parent Publication: American journal of human genetics
Issue: 6
ISSN: 0002-9297