Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in Infancy. (2016)

First Author: Diggle CP
Attributed to:  A gene therapy approach to childhood parkinsonism 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