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A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy mutations.

Haplotypes consisting of the (CTG)n repeat, as well as several flanking markers at the myotonic dystrophy (DM) locus, were analyzed in normal individuals from 25 human populations (5 African, 2 Middle Eastern, 3 European, 6 East Asian, 3 Pacific/Australo-Melanesian, and 6 Amerindian) and in five non...

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Detalhes bibliográficos
Main Authors: Tishkoff, S A, Goldman, A, Calafell, F, Speed, W C, Deinard, A S, Bonne-Tamir, B, Kidd, J R, Pakstis, A J, Jenkins, T, Kidd, K K
Formato: Artigo
Idioma:Inglês
Publicado em: 1998
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377140/
https://ncbi.nlm.nih.gov/pubmed/9585589
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