Association between NOTCH3 gene and Parkinson’s disease based on whole-exome sequencing

OBJECTIVE: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary cerebral small vessel disease caused by mutations in the NOTCH3 gene. Previous studies have established a link between NOTCH3 variants and Parkinson’s disease (PD) in terms...

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Detalles Bibliográficos
Autores principales: Zeng, Qian, Pan, Hongxu, Zhao, Yuwen, Wang, Yige, Xu, Qian, Tan, Jieqiong, Yan, Xinxiang, Li, Jinchen, Tang, Beisha, Guo, Jifeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Aging Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9780269/
https://www.ncbi.nlm.nih.gov/pubmed/36570541
http://dx.doi.org/10.3389/fnagi.2022.995330

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9780269/
https://www.ncbi.nlm.nih.gov/pubmed/36570541
http://dx.doi.org/10.3389/fnagi.2022.995330

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