CLN6 disease caused by the same mutation originating in Pakistan has varying pathology. (2013)
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.ejpn.2013.04.011
PubMed Identifier: 23735787
Publication URI: http://europepmc.org/abstract/MED/23735787
Type: Journal Article/Review
Volume: 17
Parent Publication: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Issue: 6
ISSN: 1090-3798