Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter:: exclusion of the ITPR1 gene, the human orthologue of an ataxic mouse mutant
- 31 July 2003
- journal article
- Published by Elsevier BV in Neurobiology of Disease
- Vol. 13 (2), 147-157
- https://doi.org/10.1016/s0969-9961(03)00029-9
Abstract
No abstract availableThis publication has 54 references indexed in Scilit:
- Identification of a novel SCA locus ( SCA19 ) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21Human Genetics, 2002
- Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22‐q32American Journal of Medical Genetics, 2002
- 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
- Patterns of Instability of Expanded CAG Repeats at the ERDA1 Locus in General PopulationsAmerican Journal of Human Genetics, 1999
- Mapping of a New Autosomal Dominant Spinocerebellar Ataxia to Chromosome 22American Journal of Human Genetics, 1999
- Connexin 26 mutations in hereditary non-syndromic sensorineural deafnessNature, 1997
- Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channelNature Genetics, 1997
- Ataxia and epileptic seizures in mice lacking type 1 inositol 1,4,5-trisphosphate receptorNature, 1996
- A Regulatory Mechanism That Detects Premature Nonsense Codons in T-cell Receptor Transcripts in Vivo Is Reversed by Protein Synthesis Inhibitors in VitroJournal of Biological Chemistry, 1995