Genetic and Molecular analysis of the Spinocerebellar ataxia type 7 (SCA7) disease gene
Spinocerebellar ataxia type 7 (SCA7) is a hereditary neurodegenerative disorder affecting the cerebellum, pons and retina. SCA7 patients present with gait ataxia and visual impairment as the main symptoms. Anticipation, commonly observed in SCA7 families, is a phenomenon where an earlier age at onse...
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| Format: | Doctoral Thesis |
| Language: | English |
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Umeå universitet, Medicinsk och klinisk genetik
2000
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| Online Access: | http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-1900 http://nbn-resolving.de/urn:isbn:91-7191-770-5 |