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Maile, C A and Hingst, J R and Mahalingan, K K and O'Reilly, A O and Cleasby, M E and Mickelson, J R and McCue, M E and Anderson, S M and Hurley, T D and Wojtaszewski, J F and Piercy, R J (2017) A highly prevalent equine glycogen storage disease is explained by constitutive activation of a mutant glycogen synthase. Biochimica et Biophysica Acta, 1861 (1A). pp. 3388-3398.
McCue, M E and Anderson, S M and Valberg, S J and Piercy, R J and Barakzai, S Z and Binns, M M and Distl, O and Penedo, M C T and Wagner, M L and Mickelson, J R (2010) Estimated prevalence of the Type 1 Polysaccharide Storage Myopathy mutation in selected North American and European breeds. ANIMAL GENETICS, 41 (Supp 2). pp. 145-149.