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Huntington's disease: the case for genetic modifiers
For almost three decades, Huntington's disease has been a prototype for the application of genetic strategies to human disease. HD, the Huntington's disease gene, was the first autosomal defect mapped using only DNA markers, a finding in 1983 that helped to spur similar studies in many oth...
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| Auteurs principaux: | , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
BioMed Central
2009
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2768966/ https://ncbi.nlm.nih.gov/pubmed/19725930 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gm80 |
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