Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia
- 6 December 2000
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 95 (4), 351-358
- https://doi.org/10.1002/1096-8628(20001211)95:4<351::aid-ajmg10>3.0.co;2-r
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12Nature Genetics, 1999
- Spinocerebellar ataxia type 2 in southern Italy: a clinical and molecular study of 30 families.Zeitschrift für Neurologie, 1999
- An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)Nature Genetics, 1999
- The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlatesBrain, 1998
- Analysis of the dynamic mutation in the SCA7 gene shows marked parental effects on CAG repeat transmissionHuman Molecular Genetics, 1998
- Spinocerebellar ataxia type 6: CAG repeat expansion in α1a voltage‐dependent calcium channel gene and clinical variations in japanese populationAnnals of Neurology, 1997
- Spinocerebellar ataxia type 6Neurology, 1997
- Spinocerebellar ataxia type 6Neurology, 1997
- The expansion of the CAG repeat in ataxin-2 is a frequent cause of autosomal dominant spinocerebellar ataxiaNeurology, 1997
- Frequency of the different mutations causing spinocerebellar ataxia (SCA1, SCA2, MJD/SCA3 and DRPLA) in a large group of Brazilian patientsArquivos de Neuro-Psiquiatria, 1997