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Huntington’s Disease: The Past, Present, and Future Search for Disease Modifiers
Huntington’s disease (HD) is an autosomal dominant genetic disorder that specifically causes neurodegeneration of striatal neurons, resulting in a triad of symptoms that includes emotional, cognitive, and motor disturbances. The HD mutation causes a polyglutamine repeat expansion within the N-termin...
Autor principal: | Clabough, Erin B.D. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
YJBM
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3670441/ https://www.ncbi.nlm.nih.gov/pubmed/23766742 |
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