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引文Beer, N., et al. Naturally Occurring Glucokinase Mutations at the Same Amino Acid Residue Cause Opposite Clinical Phenotypes of Hypo- and Hyperglycaemia. 2010.
警告:這些引文格式不一定是100%准確.