A carregar...
Glucocerebrosidase Defects as a Major Risk Factor for Parkinson’s Disease
Heterozygous mutations of the GBA1 gene, encoding for lysosomal enzyme glucocerebrosidase (GCase), occur in a considerable percentage of all patients with sporadic Parkinson’s disease (PD), varying between 8% and 12% across the world. Genome wide association studies have confirmed the strong correla...
Na minha lista:
| Publicado no: | Front Aging Neurosci |
|---|---|
| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2020
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7186450/ https://ncbi.nlm.nih.gov/pubmed/32372943 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnagi.2020.00097 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|