Spinocerebellar ataxias: microsatellite and allele frequency in unaffected and affected individuals.

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Compound heterozygous intermediate MJD alleles cause cerebellar ataxia with sensory neuropathy.A Comparative Optical Coherence Tomography Study of Spinocerebellar Ataxia Types 3 and 10.

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Spinocerebellar ataxias: microsatellite and allele frequency in unaffected and affected individuals.

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2009 nî lūn-bûn

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2009年の論文

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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Spinocerebellar ataxias: micro ...... cted and affected individuals.

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Spinocerebellar ataxias: micro ...... cted and affected individuals.

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Spinocerebellar ataxias: micro ...... cted and affected individuals.

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Spinocerebellar ataxias: micro ...... cted and affected individuals.

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Spinocerebellar ataxias: micro ...... cted and affected individuals.

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Spinocerebellar ataxias: micro ...... cted and affected individuals.

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Spinocerebellar ataxias: micro ...... cted and affected individuals.

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Aline Andrade Freund

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Hélio A G Teive

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Lineu Cesar Werneck

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Lupe Furtado Alle

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Magda Clara Vieira da Costa-Ribeiro

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Raquel Cristina Arndt

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Rosana Hermínia Scola

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P2860

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats

Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

Population genetics of wild-type CAG repeats in the Machado-Joseph disease gene in Portugal

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype study

A survey of spinocerebellar ataxia in South Brazil - 66 new cases with Machado-Joseph disease, SCA7, SCA8, or unidentified disease-causing mutations.

Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.

Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.

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1124-1132

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scholarly article

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10.1590/S0004-282X2009000600034

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2009-12-01T00:00:00Z

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20069235

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microsatellite

Spinocerebellar ataxias: microsatellite and allele frequency in unaffected and affected individuals.

about

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P2860

Spinocerebellar ataxias: microsatellite and allele frequency in unaffected and affected individuals.

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