Early Onset Parkinson's Disease in a family of Moroccan origin caused by a p.A217D mutation in PINK1: a case report. (2017)
Attributed to:
ERANET 1 NEURON 3: Identification of copy number variants in familial and pathologically proven PD
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1186/s12883-017-0933-z
PubMed Identifier: 28789629
Publication URI: http://europepmc.org/abstract/MED/28789629
Type: Journal Article/Review
Volume: 17
Parent Publication: BMC neurology
Issue: 1
ISSN: 1471-2377