Hunting for Familial Parkinson’s Disease Mutations in the Post Genome Era

Parkinson’s disease (PD) is typically sporadic; however, multi-incident families provide a powerful platform to discover novel genetic forms of disease. Their identification supports deciphering molecular processes leading to disease and may inform of new therapeutic targets. The LRRK2 p.G2019S muta...

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Detalles Bibliográficos
Autores principales: Bentley, Steven R., Guella, Ilaria, Sherman, Holly E., Neuendorf, Hannah M., Sykes, Alex M., Fowdar, Javed Y., Silburn, Peter A., Wood, Stephen A., Farrer, Matthew J., Mellick, George D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8002626/
https://www.ncbi.nlm.nih.gov/pubmed/33802862
http://dx.doi.org/10.3390/genes12030430

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8002626/
https://www.ncbi.nlm.nih.gov/pubmed/33802862
http://dx.doi.org/10.3390/genes12030430

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