Comprehensive assessment of PINK1 variants in Parkinson’s disease

Multiple genes have been associated with monogenic Parkinson’s disease and Parkinsonism syndromes. Mutations in PINK1 (PARK6) have been shown to result in autosomal recessive early onset Parkinson’s disease. In the past decade, several studies have suggested that carrying a single heterozygous PINK1...

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Detalhes bibliográficos
Publicado no:Neurobiol Aging
Main Authors: Krohn, Lynne, Grenn, Francis P., Makarious, Mary B., Kim, Jonggeol Jeffrey, Bandres-Ciga, Sara, Roosen, Dorien A., Gan-Or, Ziv, Nalls, Mike A., Singleton, Andrew B., Blauwendraat, Cornelis
Formato: Artigo
Idioma:Inglês
Publicado em: 2020
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7236133/
https://ncbi.nlm.nih.gov/pubmed/32249012
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neurobiolaging.2020.03.003
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