Načítá se...
Glucocerebrosidase and Parkinson disease: Recent advances
Mutations of the glucocerebrosidase (GBA) gene are the most important risk factor yet discovered for Parkinson disease (PD). Homozygous GBA mutations result in Gaucher disease (GD), a lysosomal storage disorder. Heterozygous mutations have not until recently been thought to be associated with any pa...
Uloženo v:
| Vydáno v: | Mol Cell Neurosci |
|---|---|
| Hlavní autor: | |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2015
|
| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4471139/ https://ncbi.nlm.nih.gov/pubmed/25802027 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mcn.2015.03.013 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|