Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease

BACKGROUND: Mitochondrial function is impaired in Parkinson's disease (PD) and may contribute to the pathogenesis of PD, but the causes of mitochondrial impairment in PD are unknown. Mitochondrial dysfunction is recapitulated in cell lines expressing mitochondrial DNA (mtDNA) from PD patients,...

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Detalles Bibliográficos
Autores principales: Simon, David K, Pankratz, Nathan, Kissell, Diane K, Pauciulo, Michael W, Halter, Cheryl A, Rudolph, Alice, Pfeiffer, Ronald F, Nichols, William C, Foroud, Tatiana
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2858137/
https://www.ncbi.nlm.nih.gov/pubmed/20356410
http://dx.doi.org/10.1186/1471-2350-11-53

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2858137/
https://www.ncbi.nlm.nih.gov/pubmed/20356410
http://dx.doi.org/10.1186/1471-2350-11-53

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