Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease

Background: Mitochondrial dysfunction plays a key role in PD, but the underlying molecular mechanisms remain unresolved. We hypothesized that the disruption of mitochondrial function in PD is primed by rare, protein‐altering variation in nuclear genes controlling mitochondrial structure and function...

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Detalhes bibliográficos
Publicado no:Mov Disord
Main Authors: Gaare, Johannes J., Nido, Gonzalo S., Sztromwasser, Paweł, Knappskog, Per M., Dahl, Olav, Lund‐Johansen, Morten, Maple‐Grødem, Jodi, Alves, Guido, Tysnes, Ole‐Bjørn, Johansson, Stefan, Haugarvoll, Kristoffer, Tzoulis, Charalampos
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2018
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6282592/
https://ncbi.nlm.nih.gov/pubmed/30256453
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mds.64
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