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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Baine, Fiona K, Kay, Chris, Ketelaar, Maria E, Collins, Jennifer A, Semaka, Alicia, Doty, Crystal N, Krause, Amanda, Jacquie Greenberg, L, Hayden, Michael R
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Nature Publishing Group 2013
Gaiak:
Article
Sarrera elektronikoa: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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