Evaluation of the Role of LRRK2 Gene in Parkinson’s Disease in an East Indian Cohort

Leucine rich repeat kinase 2 (LRRK2) gene defects cause Parkinson's disease (PD). Recently, LRRK2 has also been shown by genome wide association (GWA) studies to be a susceptibility gene for the disease. In India mutations in LRRK2 is a rare cause of PD. We, therefore, genotyped 64 SNPs across...

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Main Authors: Sadhukhan, Tamal, Vishal, Mansi, Das, Gautami, Sharma, Aanchal, Mukhopadhyay, Arijit, Das, Shyamal K, Ray, Kunal, Ray, Jharna
Formato: Artigo
Idioma:Inglês
Publicado: IOS Press 2012
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3826742/
https://ncbi.nlm.nih.gov/pubmed/22684232
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/DMA-2012-0898
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