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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Autores principales: Scott M Friedlander, Amanda L Herrmann, Daniel P Lowry, Emily R Mepham, Monkol Lek, Kathryn N North, Chris L Organ
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2013
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Acceso en línea:https://doaj.org/article/207bcab96376445091b065af3f3ae061
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