Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation
- Madero-Pérez, J.
- Fdez, E.
- Fernández, B.
- Lara Ordóñez, A.J.
- Blanca Ramírez, M.
- Gómez-Suaga, P.
- Waschbüsch, D.
- Lobbestael, E.
- Baekelandt, V.
- Nairn, A.C.
- Ruiz-Martínez, J.
- Aiastui, A.
- López De Munain, A.
- Lis, P.
- Comptdaer, T.
- Taymans, J.-M.
- Chartier-Harlin, M.-C.
- Beilina, A.
- Gonnelli, A.
- Cookson, M.R.
- Greggio, E.
- Hilfiker, S.
Aldizkaria:
Molecular Neurodegeneration
ISSN: 1750-1326
Argitalpen urtea: 2018
Alea: 13
Zenbakia: 1
Mota: Artikulua
