Spinocerebellar Ataxia Type 6 Mutation Alters P-type Calcium Channel Function

This publication has 34 references indexed in Scilit:

• Single Tottering Mutations Responsible for the Neuropathic Phenotype of the P-type Calcium Channel
  Journal of Biological Chemistry, 1998
• Familial Hemiplegic Migraine Mutations Change α1ACa2+ Channel Kinetics
  Published by Elsevier ,1998
• Japanese Families with Autosomal Dominant Pure Cerebellar Ataxia Map to Chromosome 19p13.1-p13.2 and Are Strongly Associated with Mild CAG Expansions in the Spinocerebellar Ataxia Type 6 Gene in Chromosome 19p13.1
  American Journal of Human Genetics, 1997
• Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel
  Nature Genetics, 1997
• Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats
  Nature Genetics, 1996
• Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT
  Nature Genetics, 1996
• Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2
  Nature Genetics, 1996
• Dominantly inherited cerebello‐olivary atrophy is not due to a mutation at the spinocerebellar ataxia‐I, machado‐joseph disease, or dentato‐rubro‐pallido‐luysian atrophy locus
  Movement Disorders, 1996
• Molecular Determinants of Calcium-Dependent Inactivation in Cardiac L-Type Calcium Channels
  Biochemical and Biophysical Research Communications, 1994
• A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
  Cell, 1993