A case of late onset sporadic Parkinson’s disease with an A53T mutation in α-synuclein

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Bibliographic Details
Published in:	Journal of neurology, neurosurgery and psychiatry Vol. 76; no. 4; pp. 596 - 597
Main Authors:	Michell, A W, Barker, R A, Raha-Chowdhury, R, Raha, S K
Format:	Journal Article
Language:	English
Published:	England BMJ Publishing Group Ltd 01-04-2005 BMJ Group
Subjects:	A53T Age Factors Aged alpha-Synuclein DNA Primers - genetics Fatal Outcome Humans Letter Levodopa - therapeutic use Male Nerve Tissue Proteins - genetics Parkinson Disease - drug therapy Parkinson Disease - genetics Parkinson’s disease Periodicity Point Mutation - genetics Polymerase Chain Reaction Synucleins α-synuclein
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Bibliography:	ark:/67375/NVC-CV446CL3-3 href:jnnp-76-596.pdf PMID:15774457 local:0760596 Correspondence to:  Dr Andrew Michell  Cambridge Centre for Brain Repair, Forvie Site, Robinson Way, Cambridge CB2 2PY, UK; awm13@cam.ac.uk istex:83A7B368F8FC29961DD4CA56AB55109EA089507E
ISSN:	0022-3050 1468-330X
DOI:	10.1136/jnnp.2004.046425