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Molecular Pathogenesis and Cellular Pathology of Spinocerebellar Ataxia Type 7 Neurodegeneration
Spinocerebellar ataxia type 7 (SCA7) is unique among CAG / polyglutamine (polyQ) repeat diseases due to dramatic intergenerational instability in repeat length and an associated cone-rod dystrophy retinal degeneration phenotype. SCA7 is caused by a polyQ expansion in the protein ataxin-7. Like other...
Wedi'i Gadw mewn:
| Prif Awduron: | , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
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2008
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| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4195584/ https://ncbi.nlm.nih.gov/pubmed/18418675 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12311-008-0027-y |
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