Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the likely disruption of FOXA2 https://www.medrxiv.org/content/10.1101/2023.08.16.23294161
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the likely disruption of FOXA2 https://www.medrxiv.org/content/10.1101/2023.08.16.23294161