Beer, N., Tribble, N., Colclough, K., Arundel, P., Grimsby, J., Chik, C., . . . Gloyn, A. (2010). Naturally occurring glucokinase mutations at the same amino acid residue cause opposite clinical phenotypes of hypo- and hyperglycaemia.
Citace podle Chicago (17th ed.)Beer, N., N. Tribble, K. Colclough, P. Arundel, J. Grimsby, C. Chik, S. Ellard, a A. Gloyn. Naturally Occurring Glucokinase Mutations at the Same Amino Acid Residue Cause Opposite Clinical Phenotypes of Hypo- and Hyperglycaemia. 2010.
Citace podle MLA (9th ed.)Beer, N., et al. Naturally Occurring Glucokinase Mutations at the Same Amino Acid Residue Cause Opposite Clinical Phenotypes of Hypo- and Hyperglycaemia. 2010.
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