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.
Chicago Style (17th ed.) CitationBeer, N., N. Tribble, K. Colclough, P. Arundel, J. Grimsby, C. Chik, S. Ellard, and A. Gloyn. Naturally Occurring Glucokinase Mutations at the Same Amino Acid Residue Cause Opposite Clinical Phenotypes of Hypo- and Hyperglycaemia. 2010.
MLA citiranjeBeer, N., et al. Naturally Occurring Glucokinase Mutations at the Same Amino Acid Residue Cause Opposite Clinical Phenotypes of Hypo- and Hyperglycaemia. 2010.
Opozorilo: Ti citati niso vedno 100% točni.