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

Internet

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

Ejemplares similares