טוען...
Ser(P)-1292 LRRK2 in Urinary Exosomes is Elevated in Idiopathic Parkinson Disease
BACKGROUND: Mutations in Leucine-rich repeat kinase 2 (LRRK2) enhance levels of autophosphorylated LRRK2 protein and are the most common known cause of inherited Parkinson disease (PD). LRRK2 has been further implicated in susceptibility to idiopathic PD in genetic association studies. OBJECTIVE: To...
שמור ב:
| הוצא לאור ב: | Mov Disord |
|---|---|
| Main Authors: | , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2016
|
| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5053851/ https://ncbi.nlm.nih.gov/pubmed/27297049 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mds.26686 |
| תגים: |
הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
|