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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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Bibliografski detalji
Glavni autori: Baine, Fiona K, Kay, Chris, Ketelaar, Maria E, Collins, Jennifer A, Semaka, Alicia, Doty, Crystal N, Krause, Amanda, Jacquie Greenberg, L, Hayden, Michael R
Format: Artigo
Jezik:Inglês
Izdano: Nature Publishing Group 2013
Teme:
Online pristup: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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