Mutations in PNKP cause recessive ataxia with oculomotor apraxia type 4. (2015)
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/10.1016/j.ajhg.2015.01.005
PubMed Identifier: 25728773
Publication URI: http://europepmc.org/abstract/MED/25728773
Type: Journal Article/Review
Volume: 96
Parent Publication: American journal of human genetics
Issue: 3
ISSN: 0002-9297