Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
Zhuchenko, O
Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel. [electronic resource] - Nature genetics Jan 1997 - 62-9 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.
1061-4036
10.1038/ng0197-62 doi
Alleles
Amino Acid Sequence
Animals
Calcium Channels--genetics
Cerebellar Ataxia--genetics
Female
Genes, Dominant
Genotype
Humans
Male
Molecular Sequence Data
Mutation
Nerve Tissue Proteins--genetics
Pedigree
Peptides--genetics
Rabbits
Sequence Homology, Amino Acid
Trinucleotide Repeats
Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel. [electronic resource] - Nature genetics Jan 1997 - 62-9 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.
1061-4036
10.1038/ng0197-62 doi
Alleles
Amino Acid Sequence
Animals
Calcium Channels--genetics
Cerebellar Ataxia--genetics
Female
Genes, Dominant
Genotype
Humans
Male
Molecular Sequence Data
Mutation
Nerve Tissue Proteins--genetics
Pedigree
Peptides--genetics
Rabbits
Sequence Homology, Amino Acid
Trinucleotide Repeats