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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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