Metadata of CSIR Papers
View Archive Info| Field | Value | |
| Creator |
Biswas, A
Sadhukhan, T Majumder, S Misra, AK Das, SK Ray, K Ray, J |
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| Subject |
Neurosciences & Neurology
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| Description |
Mutations in PINK! have been identified in familial and sporadic cases of early onset Parkinson's disease (PD) To determine the contribution of PINK1 variants in Indian PD patients, the gene was screened in 250 patients and 205 ethnically matched controls by polymerase chain reaction, single-stranded conformation polymorphism and DNA sequencing Two potentially pathogenic variants (Arg246Gln & Arg276Gln) were detected in the heterozygous state in 5 patients, none of the patients carried homozygous or compound heterozygous mutations In addition. 13 other variants were identified. including a known polymorphism (Ala340Thr). a few synonymous or intronic changes, none of which are likely to be pathogenic Unlike the Chinese population, the Ala340Thr variant did not show any association with PD in Indian population. Six single nucleotide polymorphisms (SNPs) selected from dbSNP were genotyped in 531 normal, healthy individuals representing different ethnic groups of India Most of the SNP markers were observed to be highly heterozygous among Indians. which could be used for segregation analysis of PINK1 alleles in familial PD cases (C) 2009 Elsevier Ltd All rights reserved
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| Publisher |
ELSEVIER SCI LTDOXFORDTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, OXON, ENGLAND
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| Date |
2011-09-20T12:07:10Z
2011-09-20T12:07:10Z 2010 |
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| Type |
Article
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| Identifier |
PARKINSONISM & RELATED DISORDERS
1353-8020 http://hdl.handle.net/123456789/13137 |
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| Language |
English
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