📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

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