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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2004-2-17
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pubmed:abstractText |
Spinocerebellar ataxia type 2 (SCA2) has been reported as the commonest dominant hereditary ataxia in India. However, India is an ethnically and religiously diverse population. Previous studies have not clearly indicated exact ethnic and religious origins, and must therefore be interpreted with caution. The purpose of this study was to determine the prevalence of different SCA mutations in a relatively homogeneous population from eastern India.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/14966163-10353790,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14966163-10573020,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14966163-10746559,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14966163-10942107,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14966163-11761478,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14966163-11886365,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14966163-1620135,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14966163-5571047,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14966163-6388271,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14966163-7485178,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14966163-8421964,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14966163-8896555,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14966163-9106530,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14966163-9549522,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14966163-9588855,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14966163-9758625,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14966163-9874485
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0022-3050
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
75
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
448-52
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:14966163-Adolescent,
pubmed-meshheading:14966163-Adult,
pubmed-meshheading:14966163-Age of Onset,
pubmed-meshheading:14966163-Child,
pubmed-meshheading:14966163-DNA Mutational Analysis,
pubmed-meshheading:14966163-Female,
pubmed-meshheading:14966163-Genetics, Population,
pubmed-meshheading:14966163-Genotype,
pubmed-meshheading:14966163-Haplotypes,
pubmed-meshheading:14966163-Humans,
pubmed-meshheading:14966163-India,
pubmed-meshheading:14966163-Male,
pubmed-meshheading:14966163-Nerve Tissue Proteins,
pubmed-meshheading:14966163-Pedigree,
pubmed-meshheading:14966163-Prevalence,
pubmed-meshheading:14966163-Proteins,
pubmed-meshheading:14966163-Saccades,
pubmed-meshheading:14966163-Spinocerebellar Ataxias
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pubmed:year |
2004
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pubmed:articleTitle |
Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India.
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pubmed:affiliation |
Department of Clinical Neurology, Institute of Neurology, Queen Square, London WC1N 3BG, UK.
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pubmed:publicationType |
Journal Article
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