PUBLICACIÓN

Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation

Logo Open Access

ACCEDER A LA PUBLICACIÓN: Scopus

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


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