PUBLICACIÓN
Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation
Madero-Perez J. et al.
2018 Molecular Neurodegeneration
Cellular and Molecular Neuroscience (Q1), Molecular Biology (Q1), Neurology (clinical) (Q1)
JCR: 8.274
SJR: 3.988
CITAS
72
DOI
10.1186/s13024-018-0235-y
EID
2-s2.0-85040921677
EISSN
1750-1326
AUTORES DE LA UEX