Associated Papers
Re-analysis of gene mutations found in pituitary stalk interruption syndrome and a new hypothesis on the etiology.
Wang S et al.
Frontiers in Endocrinology, 2024
Syndromic forms of congenital hyperinsulinism.
Zenker M et al.
Frontiers in Endocrinology, 2023
37065762 (PubMed )
Supplement: Table_1.xlsx › FOXA2
Novel genes and variants associated with congenital pituitary hormone deficiency in the era of next-generation sequencing.
Bando H et al.
Frontiers in Endocrinology, 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
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