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Absence/rarity of commonly reported LRRK2 mutations in Indian Parkinson's disease patients

✍ Scribed by Sohan Punia; Madhuri Behari; Shyla T. Govindappa; Pazhayannur V. Swaminath; Sachi Jayaram; Vinay Goyal; Uday B. Muthane; R.C. Juyal; B.K. Thelma

Book ID: 116768723
Publisher: Elsevier Science
Year: 2006
Tongue: English
Weight: 166 KB
Volume: 409
Category: Article
ISSN: 0304-3940
DOI: 10.1016/j.neulet.2006.04.052

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## Abstract Mutations in the leucine‐rich repeat kinase 2 (__LRRK2__) gene are the most common genetic determinant of Parkinson's disease (PD) in European‐derived populations, but far less is known about __LRRK2__ mutations and susceptibility alleles in Asians. To address this issue, we sequenced t