A clinical and family history study of Parkinson's disease in heterozygous glucocerebrosidase mutation carriers

Detalles Bibliográficos
Autores principales: McNeill, Alisdair, Duran, Raquel, Hughes, Derralynn A, Mehta, Atul, Schapira, Anthony H V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Group 2012
Materias:
PostScript
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927562/
https://www.ncbi.nlm.nih.gov/pubmed/22577228
http://dx.doi.org/10.1136/jnnp-2012-302402
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author McNeill, Alisdair
Duran, Raquel
Hughes, Derralynn A
Mehta, Atul
Schapira, Anthony H V
author_facet McNeill, Alisdair
Duran, Raquel
Hughes, Derralynn A
Mehta, Atul
Schapira, Anthony H V
author_sort McNeill, Alisdair
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spelling pubmed-39275622014-02-25 A clinical and family history study of Parkinson's disease in heterozygous glucocerebrosidase mutation carriers McNeill, Alisdair Duran, Raquel Hughes, Derralynn A Mehta, Atul Schapira, Anthony H V J Neurol Neurosurg Psychiatry PostScript BMJ Group 2012-05-10 2012-08 /pmc/articles/PMC3927562/ /pubmed/22577228 http://dx.doi.org/10.1136/jnnp-2012-302402 Text en © 2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/
spellingShingle PostScript
McNeill, Alisdair
Duran, Raquel
Hughes, Derralynn A
Mehta, Atul
Schapira, Anthony H V
A clinical and family history study of Parkinson's disease in heterozygous glucocerebrosidase mutation carriers
title A clinical and family history study of Parkinson's disease in heterozygous glucocerebrosidase mutation carriers
title_full A clinical and family history study of Parkinson's disease in heterozygous glucocerebrosidase mutation carriers
title_fullStr A clinical and family history study of Parkinson's disease in heterozygous glucocerebrosidase mutation carriers
title_full_unstemmed A clinical and family history study of Parkinson's disease in heterozygous glucocerebrosidase mutation carriers
title_short A clinical and family history study of Parkinson's disease in heterozygous glucocerebrosidase mutation carriers
title_sort clinical and family history study of parkinson's disease in heterozygous glucocerebrosidase mutation carriers
topic PostScript
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927562/
https://www.ncbi.nlm.nih.gov/pubmed/22577228
http://dx.doi.org/10.1136/jnnp-2012-302402
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