Parkinson disease, juvenile, type 2
OMIM:600116Mode of inheritance:Autosomal recessive
Disease classification:Diseases of the nervous system
Mutations
Gene Symbol | PARK2 |
---|---|
Reference transcript | NM_004562.2 |
DNA Change | c.871delG |
A.A. Change | p.Ala291Leufs*7 |
Exon/Intron | exon 7 |
Mutation Type | deletion |
Reference | Munoz E, Pastor P, Marti MJ, Oliva R, Tolosa E.A new mutation in the parkin gene in a patient with atypical autosomal recessive juvenile parkinsonism. Neurosci Lett. 2000 Jul 28;289(1):66-8. |