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Article

Evaluation of the role of LRRK2 gene in Parkinson's disease in an East Indian cohort.

Disease markers - 1 Jan 2012

Sadhukhan Tamal, Vishal Mansi, Das Gautami, Sharma Aanchal, Mukhopadhyay Arijit, Das Shyamal K, Ray Kunal, Ray Jharna

Abstract excerpt

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 LRRK2 in 161 control samples and finally studied 6 haplotype tagging SNPs for association-based study on 300 cases and...

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Identifiers

PMID: 22684232
DOI: 10.3233/DMA-2012-0898
PMCID: PMC3826742

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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