Genetic & Genomic MedicineEuropean Journal of Human GeneticsPeer-reviewed
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the likely disruption of FOXA2
Thomas William Laver, Matthew Neil Wakeling, Richard C. Caswell…·Sarah Elizabeth Flanagan
The paper identifies chromosome 20p11.2 deletions as a cause of congenital hyperinsulinism by disrupting FOXA2 expression in pancreatic beta-cells.
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