Study of the collagen type VI alpha 3 (COL6A3) gene in Parkinson’s disease

BACKGROUND: To date, the genetic contribution to Parkinson’s disease (PD) remains unclear. Mutations in the collagen type VI alpha 3 (COL6A3) gene were recently identified as a cause of isolated dystonia. Since PD and dystonia are closely related disorders with shared clinical and genetic characteri...

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Detalles Bibliográficos
Autores principales: Jin, Chong-Yao, Zheng, Ran, Lin, Zhi-Hao, Xue, Nai-Jia, Chen, Ying, Gao, Ting, Yan, Yi-Qun, Fang, Yi, Yan, Ya-Ping, Yin, Xin-Zhen, Tian, Jun, Pu, Jia-Li, Zhang, Bao-Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8106155/
https://www.ncbi.nlm.nih.gov/pubmed/33964895
http://dx.doi.org/10.1186/s12883-021-02215-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8106155/
https://www.ncbi.nlm.nih.gov/pubmed/33964895
http://dx.doi.org/10.1186/s12883-021-02215-7

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