No abstract available
MeSH terms
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Adult
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Ataxia / genetics
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DNA / genetics*
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Female
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Fragile X Syndrome / genetics
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Humans
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Huntington Disease / genetics
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Infant, Newborn
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Male
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Muscular Atrophy, Spinal / genetics
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Mutation
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Myotonic Dystrophy / genetics
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Nervous System Diseases / genetics*
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Trinucleotide Repeats*