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ACTN3 Allele Frequency in Humans Covaries with Global Latitudinal Gradient

A premature stop codon in ACTN3 resulting in α-actinin-3 deficiency (the ACTN3 577XX genotype) is common in humans and reduces strength, muscle mass, and fast-twitch fiber diameter, but increases the metabolic efficiency of skeletal muscle. Linkage disequilibrium data suggest that the ACTN3 R577X al...

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Autors principals: Friedlander, Scott M., Herrmann, Amanda L., Lowry, Daniel P., Mepham, Emily R., Lek, Monkol, North, Kathryn N., Organ, Chris L.
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2013
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3554748/
https://ncbi.nlm.nih.gov/pubmed/23359641
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0052282
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