Name

Fam2 (1 documented family member)

Phenotype

Parkinson's disease

Inheritance

Autosomal Dominant

Onset Age

(2 patients)

Age at Death

Ethnic origin

Caucasian (France or Italy)

Mutation

SNCA dupSNCA[ P2]

Citations

Ibáñez P, Lancet 364: 1169-71, 2004

Added: April 27, 2009

ID: 22