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Neurosci Lett ; 523(2): 145-7, 2012 Aug 15.
Article in English | MEDLINE | ID: mdl-22766139

ABSTRACT

With the etiology being unclear till date, a combination of age, genetic and environmental factors are known to play a significant role in the pathogenesis of Parkinson's disease. Mutations in PARK2 gene have been implicated to cause autosomal recessive early onset PD. We analyzed the 12 coding exons of PARK2 gene in 16 early onset PD patients of South Indian ethnicity. PARK2 mutations were present in 68% of the early onset cases. We report the presence of four PARK2 sequence variants c.1239G>C, c.171+25T>C, c.202A>G, c.601G>A, and a novel insertion mutation, c.798_799insA in the exon 7 of PARK2 gene. These results suggest that mutations in PARK2 gene may be a common cause of PD among South Indian early onset patients.


Subject(s)
Parkinson Disease/genetics , Ubiquitin-Protein Ligases/genetics , Adult , Age of Onset , Female , Genetic Association Studies , Genetic Predisposition to Disease , Humans , India , Male , Middle Aged , Mutation , Parkinson Disease/ethnology
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