Identification of BAG5 as a Potential Biomarker for Parkinson’s Disease Patients With R492X PINK1 Mutation

Parkinson’s disease (PD) is a degenerative, progressive nervous system disorder with an unknown cause. PINK1 [phosphatase and tensin homolog deleted on chromosome 10 (PTEN)-induced putative kinase 1] causative mutations R492X may cause autosomal recessive early-onset parkinsonism. In this study, we...

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Detalles Bibliográficos
Autores principales: Fu, Yu, Chen, Yongkang, Tian, Haiyan, Liu, Han, Qi, Dan, Wu, Erxi, Wang, Xuejing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9363588/
https://www.ncbi.nlm.nih.gov/pubmed/35968372
http://dx.doi.org/10.3389/fnins.2022.903958

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9363588/
https://www.ncbi.nlm.nih.gov/pubmed/35968372
http://dx.doi.org/10.3389/fnins.2022.903958

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