Modelling the functional genomics of Parkinson’s disease in Caenorhabditis elegans: LRRK2 and beyond

For decades, Parkinson’s disease (PD) cases have been genetically categorised into familial, when caused by mutations in single genes with a clear inheritance pattern in affected families, or idiopathic, in the absence of an evident monogenic determinant. Recently, genome-wide association studies (G...

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Detalles Bibliográficos
Autores principales: Chandler, Rachael J., Cogo, Susanna, Lewis, Patrick A., Kevei, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2021
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8415217/
https://www.ncbi.nlm.nih.gov/pubmed/34397087
http://dx.doi.org/10.1042/BSR20203672

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8415217/
https://www.ncbi.nlm.nih.gov/pubmed/34397087
http://dx.doi.org/10.1042/BSR20203672

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