Koster, J. C., Cadario, F., Peruzzi, C., Colombo, C., Nichols, C. G., & Barbetti, F. (2008). The G53D Mutation in Kir6.2 (KCNJ11) Is Associated with Neonatal Diabetes and Motor Dysfunction in Adulthood that Is Improved with Sulfonylurea Therapy. The Endocrine Society.
Stile di citazione ChicagoKoster, Joseph C., Francesco Cadario, Cinzia Peruzzi, Carlo Colombo, Colin G. Nichols, e Fabrizio Barbetti. The G53D Mutation in Kir6.2 (KCNJ11) Is Associated With Neonatal Diabetes and Motor Dysfunction in Adulthood That Is Improved With Sulfonylurea Therapy. The Endocrine Society, 2008.
Citazione MLAKoster, Joseph C., et al. The G53D Mutation in Kir6.2 (KCNJ11) Is Associated With Neonatal Diabetes and Motor Dysfunction in Adulthood That Is Improved With Sulfonylurea Therapy. The Endocrine Society, 2008.