Glucocerebrosidase Enzyme Activity in GBA Mutation Parkinson Disease

Mutations in the glucocerebrosidase (GBA1) gene, the most common genetic contributor to Parkinson’s disease (PD), are associated with an increased risk of PD in heterozygous and homozygous carriers. While glucocerebrosidase enzyme (GCase) activity is consistently low in Gaucher disease, there is a r...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:J Clin Neurosci
Main Authors: Ortega, Roberto A., Torres, Paola A., Swan, Matthew, Nichols, William, Boschung, Sarah, Raymond, Deborah, Barrett, Matthew J., Johannes, Brooke A., Severt, Lawrence, Shanker, Vicki, Hunt, Ann L., Bressman, Susan, Pastores, Gregory M., Saunders-Pullman, Rachel
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4856562/
https://ncbi.nlm.nih.gov/pubmed/26857292
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jocn.2015.12.004
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados