Allelic variant in SLC6A3 rs393795 affects cerebral regional homogeneity and gait dysfunction in patients with Parkinson’s disease

AIMS: We sought to explore the role of the SLC6A3 rs393795 allelic variant in cerebral spontaneous activity and clinical features in Parkinson’s disease (PD) via imaging genetic approach. METHODS: Our study recruited 50 PD and 45 healthy control (HC) participants to provide clinical, genetic, and re...

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Detalles Bibliográficos
Autores principales: Wang, Lina, Yuan, Yongsheng, Wang, Jianwei, Shen, Yuting, Zhi, Yan, Li, Junyi, Wang, Min, Zhang, Kezhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2019
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6836753/
https://www.ncbi.nlm.nih.gov/pubmed/31720106
http://dx.doi.org/10.7717/peerj.7957

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6836753/
https://www.ncbi.nlm.nih.gov/pubmed/31720106
http://dx.doi.org/10.7717/peerj.7957

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