Permanent Neonatal Diabetes Mellitus Caused by a Novel Homozygous (T168A) Glucokinase (GCK) Mutation: Initial Response to Oral Sulphonylurea Therapy
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference16 articles.
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3. Activating mutations in the gene encoding Kir6.2 alter fetal and postnatal growth and also cause neonatal diabetes;Slingerland;J Clin Endocrinol Metab,2006
4. Insulin promoter factor-1 gene mutation linked to early-onset type 2 diabetes mellitus directs expression of a dominant negative isoprotein;Stoffers;J Clin Invest,1998
5. Neonatal diabetes mellitus due to complete glucokinase deficiency;Njolstad;N Engl J Med,2001
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1. Glucokinase (GCK) in diabetes: from molecular mechanisms to disease pathogenesis;Cellular & Molecular Biology Letters;2024-09-08
2. Pathogenesis (of Neonatal Diabetes and Early Onset Diabetes);Neonatal and Early Onset Diabetes Mellitus;2023
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4. Neonatal diabetes onset mimicking an organic acidemia;Endocrinología, Diabetes y Nutrición;2022-02
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