Exploring the Genotype–Phenotype Correlation in GBA-Parkinson Disease: Clinical Aspects, Biomarkers, and Potential Modifiers

Variants in the glucocerebrosidase (GBA) gene are the most common genetic risk factor for Parkinson disease (PD). These include pathogenic variants causing Gaucher disease (GD) (divided into “severe,” “mild,” or “complex”—resulting from recombinant alleles—based on the phenotypic effects in GD) and...

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Detalles Bibliográficos
Autores principales: Menozzi, Elisa, Schapira, Anthony H. V.
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/PMC8264189/
https://www.ncbi.nlm.nih.gov/pubmed/34248830
http://dx.doi.org/10.3389/fneur.2021.694764

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8264189/
https://www.ncbi.nlm.nih.gov/pubmed/34248830
http://dx.doi.org/10.3389/fneur.2021.694764

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