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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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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1998
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377140/
https://ncbi.nlm.nih.gov/pubmed/9585589
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