SNP information rs33939927
Normal allele: CC
Mutation in LRRK2 causes autosomal dominant parkinsonism with pleomorphic pathology.
Polymorphism rs33939927 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:
7898705 Western Nebraska family (family D) with autosomal dominant parkinsonism.
15541308 Cloning of a gene containing mutations causing PARK8-related Parkinson's disease.
15541309 Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.
16003110 Genetics of Parkinson's disease.
16269541 Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 increase kinase activity.
19667187 R1441C mutation in LRRK2 impairs dopaminergic neurotransmission in mice.
20301387 LRRK2 Parkinson Disease.
21885347 Association of LRRK2 exonic variants with Parkinson's disease susceptibility: a case-control study.
The presence of lesions on the brain and spinal cord is indicative of multiple sclerosis, a...
Dementia is characterized as a syndrome, rather than a singular disease. Individuals with early...
Alzheimer's disease is a degenerative brain disease that causes dementia, resulting in a gradual...