Assessing the relationship between monoallelic PRKN mutations and Parkinson’s risk

Biallelic Parkin (PRKN) mutations cause autosomal recessive Parkinson’s disease (PD); however, the role of monoallelic PRKN mutations as a risk factor for PD remains unclear. We investigated the role of single heterozygous PRKN mutations in three large independent case-control cohorts totalling 10 8...

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Detalles Bibliográficos
Autores principales: Lubbe, Steven J, Bustos, Bernabe I, Hu, Jing, Krainc, Dimitri, Joseph, Theresita, Hehir, Jason, Tan, Manuela, Zhang, Weijia, Escott-Price, Valentina, Williams, Nigel M, Blauwendraat, Cornelis, Singleton, Andrew B, Morris, Huw R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
General Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033143/
https://www.ncbi.nlm.nih.gov/pubmed/33448283
http://dx.doi.org/10.1093/hmg/ddaa273

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033143/
https://www.ncbi.nlm.nih.gov/pubmed/33448283
http://dx.doi.org/10.1093/hmg/ddaa273

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