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spinocerebellar ataxia type 19 (SCA-19)

Epidemiology: - single Dutch family Genetics: - linked to gene on chromosome 1p21-q21 (region overlaps with SCA22) Clinical manifestations: 1) mild cerebellar ataxia 2) myoclonus 3) tremor

General

spinocerebellar ataxia (SCA)

Database Correlations

OMIM 607346 Entrez Gene 140452

References

  1. Duenas AM et al, Molecular pathogenesis of spinocerebellar ataxias. Brain. 2006, 120:1357 PMID: 16613893
  2. Koeppen AH et al, The pathogenesis of spinocerebellar ataxia. Cerebellum 2005, 4:62 PMID: 15895563
  3. UpToDate version 14.2
  4. PubMed Search PubMed search: spinocerebellar+ataxia+type+19