Clinical Variability of SYNJ1-Associated Early-Onset Parkinsonism

Autosomal recessive early-onset parkinsonism is clinically and genetically heterogeneous. Mutations of three genes, PRKN, PINK1, and DJ-1 cause pure phenotypes usually characterized by levodopa-responsive Parkinson's disease. By contrast, mutations of other genes, including ATP13A2, PLA2G6, FBX...

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Detalles Bibliográficos
Autores principales: Lesage, Suzanne, Mangone, Graziella, Tesson, Christelle, Bertrand, Hélène, Benmahdjoub, Mustapha, Kesraoui, Selma, Arezki, Mohamed, Singleton, Andrew, Corvol, Jean-Christophe, Brice, Alexis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027075/
https://www.ncbi.nlm.nih.gov/pubmed/33841314
http://dx.doi.org/10.3389/fneur.2021.648457

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027075/
https://www.ncbi.nlm.nih.gov/pubmed/33841314
http://dx.doi.org/10.3389/fneur.2021.648457

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