SNP information rs35808389
Normal allele: AA
Mutation in LRRK2 causes autosomal dominant parkinsonism with pleomorphic pathology.
Polymorphism rs35808389 is related to topics like this:
A disorder that progresses gradually within the nervous system is known as Parkinson's disease. It...
Research and publications:
15541309 Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.
20301387 LRRK2 Parkinson Disease.
21885347 Association of LRRK2 exonic variants with Parkinson's disease susceptibility: a case-control study.