Spinocerebellar ataxia type 17 in Indian patients: Two rare cases of homozygous expansions

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dc.contributor.authorHire, R. R.
dc.contributor.authorKatrak, S. M.
dc.contributor.authorVaidya, S.
dc.contributor.authorRadhakrishnan, K.
dc.contributor.authorSeshadri, M.
dc.date.accessioned2012-01-20T09:42:15Z
dc.date.available2012-01-20T09:42:15Z
dc.date.issued2011
dc.format.extent4170 bytes
dc.format.mimetypetext/html
dc.identifier.sourceClinical Genetics, 2011. Vol. 80 (5): pp. 472-477en
dc.identifier.urihttp://hdl.handle.net/123456789/5732
dc.language.isoenen
dc.subjectCAG/CAA repeatsen
dc.subjectChoreaen
dc.subjecthomozygousen
dc.subjectpolyglutamineen
dc.subjectspinocerebellar ataxia 17en
dc.subjectTATA-boxen
dc.subjectbinding proteinen
dc.titleSpinocerebellar ataxia type 17 in Indian patients: Two rare cases of homozygous expansionsen
dc.typeArticleen

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