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Article

A New Dominant Spinocerebellar Ataxia Linked to Chromosome 19q13.4-qter

1 Aug 2002

Abstract excerpt

BACKGROUND: The autosomal dominant spinocerebellar ataxias (SCAs) are a clinically and genetically heterogeneous group of neurodegenerative disorders. Although molecular genetic studies have so far implicated 16 loci in the etiology of these diseases, approximately 30% of families with SCAs remain unlinked. OBJECTIVES: To report the location of a gene causing a "pure" autosomal dominant cerebellar ataxia in one...

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PMID: 12164726
DOI: 10.1001/archneur.59.8.1291

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Research trail→

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A New Dominant Spinocerebellar Ataxia Linked to Chromosome 19q13.4-qterPMID 12164726Read ↗

An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?Semantic proximity Read ↗

A novel locus for dominant cerebellar ataxia (SCA14) maps to a 10.2-cM interval flanked by D19S206 and D19S605 on chromosome 19q13.4-qter.Semantic proximity Read ↗

Identification of a novel SCA locus ( SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21.Semantic proximity Read ↗

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A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3-p15.1.Semantic proximity Read ↗

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Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsy.Semantic proximity Read ↗

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