Salguero Bermonth, M. V., Letourneau-Freiberg, L., Devine, N., & Greeley, S. A. W. (2021). Inheritance of Mildly Activating ABCC8 Mutation From a Mother With MODY Causes Permanent Neonatal Diabetes Mellitus (NDM) in Two Siblings Who Also Carry a Second Inactivating Mutation: Genetic Testing Allows for Improved Treatment With Sulfonylureas (SU). J Endocr Soc.
Chicago Style CitationSalguero Bermonth, Maria Victoria, Lisa Letourneau-Freiberg, Nancy Devine, i Siri Atma W. Greeley. "Inheritance of Mildly Activating ABCC8 Mutation From a Mother With MODY Causes Permanent Neonatal Diabetes Mellitus (NDM) in Two Siblings Who Also Carry a Second Inactivating Mutation: Genetic Testing Allows for Improved Treatment With Sulfonylureas (SU)." J Endocr Soc 2021.
Cita MLASalguero Bermonth, Maria Victoria, Lisa Letourneau-Freiberg, Nancy Devine, i Siri Atma W. Greeley. "Inheritance of Mildly Activating ABCC8 Mutation From a Mother With MODY Causes Permanent Neonatal Diabetes Mellitus (NDM) in Two Siblings Who Also Carry a Second Inactivating Mutation: Genetic Testing Allows for Improved Treatment With Sulfonylureas (SU)." J Endocr Soc 2021.