Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in Infancy. (2016)
Attributed to:
Infrastructure for collaboration: Leeds MRC Medical Bioinformatics Centre
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2016.03.015
PubMed Identifier: 27058446
Publication URI: http://europepmc.org/abstract/MED/27058446
Type: Journal Article/Review
Volume: 98
Parent Publication: American journal of human genetics
Issue: 4
ISSN: 0002-9297