Abstract
We investigated 30 patients with familial essential tremor (ET) for spinocerebellar ataxia type 12 (SCA-12) mutations. No patient presented a CAG repeat larger than 19, suggesting that familial ET and SCA-12 are distinct diseases.
Copyright 2002 Movement Disorder Society
MeSH terms
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Alleles
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Chromosomes, Human, Pair 5*
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DNA Mutational Analysis
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Essential Tremor / diagnosis
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Essential Tremor / genetics*
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Female
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Genetics, Population
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Humans
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Italy
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Male
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Phosphoprotein Phosphatases / genetics
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Point Mutation / genetics*
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Protein Phosphatase 2
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Spinocerebellar Ataxias / diagnosis
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Spinocerebellar Ataxias / genetics*
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Trinucleotide Repeats / genetics
Substances
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PPP2R1B protein, human
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Ppp2r1b protein, mouse
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Phosphoprotein Phosphatases
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Protein Phosphatase 2