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Symptom onset of spinocerebellar ataxia type 10 in pregnancy and puerperium

  • Published:2011-03 Issue:3 Volume:18 Page:437-438
  • ISSN:0967-5868
  • Container-title:Journal of Clinical Neuroscience
  • language:en
  • Short-container-title:Journal of Clinical Neuroscience

Author:

Teive H.A.G.,Arruda W.O.,Raskin S.,Munhoz R.P.,Zavala J.A.,Werneck L.C.,Ashizawa T.

Publisher

Elsevier BV

Subject

Physiology (medical),Neurology (clinical),Neurology,General Medicine,Surgery

Reference14 articles.

1. The history of spinocerebellar ataxia type 10 in Brazil. Travels of a gene;Teive;Arq Neuropsiquiatr,2007

2. Prasad A, Prasad C, Jog MS. Ataxia with identified genetic and biochemical defects. eMedicine 2009. Available from: .

3. Mapping of a gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsy;Matsuura;Ann Neurol,1999

4. Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22;Zu;Am J Hum Genet,1999

5. Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10;Matsuura;Nat Genet,2000

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