Associated Papers
Syndromic forms of congenital hyperinsulinism.
Zenker M et al.
Frontiers in Endocrinology, 2023
37065762 (PubMed )
Supplement: Table_1.xlsx › FOXA2
Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract.
Zheng B et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association, 2022
Dysgenesis and Dysfunction of the Pancreas and Pituitary Due to FOXA2 Gene Defects.
Kaygusuz SB et al.
The Journal of Clinical Endocrinology and Metabolism, 2021
Exome sequencing identifies a de novo FOXA2 variant in a patient with syndromic diabetes.
Stekelenburg C et al.
Pediatric Diabetes, 2019
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