α-Synuclein (SNCA) A30G Mutation as a Cause of a Complex Phenotype Without Parkinsonism.

Subjects

Subjects :

Humans
Mutation genetics
Phenotype
Parkinsonian Disorders diagnostic imaging
Parkinsonian Disorders genetics
alpha-Synuclein genetics

Details

Language :

English

ISSN :

1531-8257

Volume :

36

Issue :

9

Database :

MEDLINE

Journal :

Movement disorders : official journal of the Movement Disorder Society

Publication Type :

Report

Accession number :

34543462

Full Text :

https://doi.org/10.1002/mds.28735