📣 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.

Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis. (2012)

First Author: Bras J

Attributed to: A systematic investigation into the pathogenesis and course of Parkinson's syndrome funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/hmg/dds089

PubMed Identifier: 22388936

Publication URI: http://europepmc.org/abstract/MED/22388936

Type: Journal Article/Review

Volume: 21

Parent Publication: Human molecular genetics

Issue: 12

ISSN: 0964-6906