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Ataxia
Trinucleotide repeat disorder
Key terms: ataxia spinocerebellar ataxia disease autosomal type disorder autosomal recessive symptoms gene dominant autosomal dominant repeat glutamine sca hereditary genetic inherited cause degeneration atrophy progressive devices onset uw entry coordination ncbi forms nih expansion gait impaired cerebellum omim cag Search external links cited by footnotes on Wikipedia page Spinocerebellar ataxia: |
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