A prevalent variant in PPP1R3A impairs glycogen synthesis and reduces muscle glycogen content in humans and mice.

BACKGROUND: Stored glycogen is an important source of energy for skeletal muscle. Human genetic disorders primarily affecting skeletal muscle glycogen turnover are well-recognised, but rare. We previously reported that a frameshift/premature stop mutation in PPP1R3A, the gene encoding RGL, a key reg...

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Detalles Bibliográficos
Main Authors:	Savage, D, Zhai, L, Ravikumar, B, Choi, C, Snaar, J, McGuire, A, Wou, SE, Medina-Gomez, G, Kim, S, Bock, C, Segvich, D, Solanky, B, Deelchand, D, Vidal-Puig, A, Wareham, N, Shulman, G, Karpe, F, Taylor, R, Pederson, B, Roach, P, O'Rahilly, S, DePaoli-Roach, A
Formato:	Journal article
Idioma:	English
Publicado:	Public Library of Science 2008

A prevalent variant in PPP1R3A impairs glycogen synthesis and reduces muscle glycogen content in humans and mice.

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