Mitochondrial DNA variation in Parkinson's disease: Analysis of "out-of-place" population variants as a risk factor.

Müller-Nedebock, Amica C; Pfaff, Abigail L; Pienaar, Ilse S; Kõks, Sulev; van der Westhuizen, Francois H; Elson, Joanna L; Bardien, Soraya

Müller-Nedebock, Amica C; Pfaff, Abigail L; Pienaar, Ilse S; Kõks, Sulev; van der Westhuizen, Francois H; Elson, Joanna L; Bardien, Soraya.

Afiliación

Müller-Nedebock AC; Division of Molecular Biology and Human Genetics, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Pfaff AL; South African Medical Research Council, Stellenbosch University Genomics of Brain Disorders Research Unit, Stellenbosch University, Cape Town, South Africa.
Pienaar IS; Perron Institute for Neurological and Translational Science, Nedlands, WA, Australia.
Kõks S; Centre for Molecular Medicine and Innovative Therapeutics, Murdoch University, Murdoch, WA, Australia.
van der Westhuizen FH; Institute of Clinical Sciences, University of Birmingham, Birmingham, United Kingdom.
Elson JL; Perron Institute for Neurological and Translational Science, Nedlands, WA, Australia.
Bardien S; Centre for Molecular Medicine and Innovative Therapeutics, Murdoch University, Murdoch, WA, Australia.

Front Aging Neurosci ; 14: 921412, 2022.

Article en En | MEDLINE | ID: mdl-35912088

Palabras clave

African ancestry; PPMI cohort; Parkinsion's disease; mitochondrial DNA; mtDNA; out-of-place variation; risk factor

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Etiology_studies / Risk_factors_studies Idioma: En Revista: Front Aging Neurosci Año: 2022 Tipo del documento: Article País de afiliación: Sudáfrica

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google