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Huntington disease in the South African population occurs on diverse and ethnically distinct genetic haplotypes
Huntington disease (HD) is a neurodegenerative disorder resulting from the expansion of a CAG trinucleotide repeat in the huntingtin (HTT) gene. Worldwide prevalence varies geographically with the highest figures reported in populations of European ancestry. HD in South Africa has been reported in C...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3778359/ https://ncbi.nlm.nih.gov/pubmed/23463025 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2013.2 |
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