Does a rare mutation in PTPRA contribute to the development of Parkinson’s disease in an Australian multi-incident family?

The genetic study of multi-incident families is a powerful tool to investigate genetic contributions to the development of Parkinson’s disease. In this study, we identified the rare PTPRA p.R223W variant as one of three putative genetic factors potentially contributing to disease in an Australian fa...

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Detalles Bibliográficos
Autores principales: Hill, Melissa A., Bentley, Steven R., Walker, Tara L., Mellick, George D., Wood, Stephen A., Sykes, Alex M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9333306/
https://www.ncbi.nlm.nih.gov/pubmed/35900966
http://dx.doi.org/10.1371/journal.pone.0271499

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9333306/
https://www.ncbi.nlm.nih.gov/pubmed/35900966
http://dx.doi.org/10.1371/journal.pone.0271499

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