SNP information rs34995376
Normal allele: GG
LRRK2 mutation associated with the development of Parkinson's disease (6.5-fold increased risk) and progressive supranuclear palsy.
Polymorphism rs34995376 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:
16157909 A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations.
16172858 Pathogenic Lrrk2 substitutions in Parkinson's disease.
17060595 LRRK2 mutations on Crete: R1441H associated with PD evolving to PSP.
18952485 Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism.
20301387 LRRK2 Parkinson Disease.
21885347 Association of LRRK2 exonic variants with Parkinson's disease susceptibility: a case-control study.
34109443 An attempt to isolate a peripheral marker based on cellular pathology in Parkinson's disease.
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