Associated Papers
Genetic variant profiling of neonatal diabetes mellitus in Iranian patients: Unveiling 58 distinct variants in 14 genes.
Mianesaz H et al.
Journal of Diabetes Investigation, 2024
MNX1 mutations causing neonatal diabetes: Review of the literature and report of a case with extra-pancreatic congenital defects presenting in severe diabetic ketoacidosis.
Aly HH et al.
Journal of Diabetes Investigation, 2023
Currarino syndrome: a comprehensive genetic review of a rare congenital disorder.
Dworschak GC et al.
Orphanet Journal of Rare Diseases, 2021
Functional Defects From Endocrine Disease-Associated Mutations in HLXB9 and Its Interacting Partner, NONO.
Kharade SS et al.
Endocrinology, 2018
Analysis of transcription factors key for mouse pancreatic development establishes NKX2-2 and MNX1 mutations as causes of neonatal diabetes in man.
Flanagan SE et al.
Cell Metabolism, 2014
Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous family.
Bonnefond A et al.
Diabetes & Metabolism, 2013
Select a paper to view details