A highly prevalent equine glycogen storage disease is explained by constitutive activation of a mutant glycogen synthase

C. A. Maile, J. R. Hingst, K. K. Mahalingan, A. O. O'Reilly, M. E. Cleasby, J. R. Mickelson, M. E. McCue, S. M. Anderson, T. D. Hurley, J. F.P. Wojtaszewski, R. J. Piercy

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Biochemistry, Genetics and Molecular Biology