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Chromosomal localization of the human genes for alpha-1A, alpha-1B, and alpha-1E voltagedependent Ca(2+) channel subunits
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An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exhange-factor domains
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Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): Clinical description and genetic localization to chromosome 16q22.1
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Autosomal dominant cerebellar ataxia type III: Linkage in a large British family to a 7.6cM region on chromosome 15q14-21.3
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Spinocerebellar ataxia type 15 (SCA15) maps to 3p24.2-4pter: Exclusion of the ITPR1 gene, the human orthologue of an ataxic mouse mutant
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A novel, heritable, expanding CTG repeat in an intron of the SEF2-1 gene on chromosome 18q21.1
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