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Early Onset Parkinson's Disease in a family of Moroccan origin caused by a p.A217D mutation in PINK1: a case report. (2017)

First Author: Norman BP

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