Regional features of autosomal-dominant cerebellar ataxia in Nagano: clinical and molecular genetic analysis of 86 families
Open Access
- 8 October 2004
- journal article
- research article
- Published by Springer Nature in Journal of Human Genetics
- Vol. 49 (11) , 610-616
- https://doi.org/10.1007/s10038-004-0196-6
Abstract
No abstract availableKeywords
This publication has 37 references indexed in Scilit:
- Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2pAnnals of Neurology, 2003
- Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter:Neurobiology of Disease, 2003
- Identification of a novel SCA locus ( SCA19 ) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21Human Genetics, 2002
- A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3‐p15.1Annals of Neurology, 2002
- A linkage disequilibrium at the candidate gene locus for 16q-linked autosomal dominant cerebellar ataxia type III in JapanJournal of Human Genetics, 2001
- Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10Nature Genetics, 2000
- Autosomal Dominant Cerebellar Ataxia Type III: Linkage in a Large British Family to a 7.6-cM Region on Chromosome 15q14-21.3American Journal of Human Genetics, 1999
- Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channelNature Genetics, 1997
- Coexistence of type I familial amyloid polyneuropathy and spinocerebellar ataxia type 1. Clinical and genetic studies of a Japanese family.Journal of Neurology, Neurosurgery & Psychiatry, 1996
- Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11Nature Genetics, 1994