Publication 9917
Title:Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements
Journal:European Journal of Human Genetics
Published:11 Apr 2024
Pubmed:https://pubmed.ncbi.nlm.nih.gov/38605124/
DOI:https://doi.org/10.1038/s41431-024-01593-z
URL:https://www.nature.com/articles/s41431-024-01593-z.pdf
Citations:1 (1 in last 2 years) as of 8 Aug 2024