Associated Papers
Homozygosity for a variant in SLC10A2 and infancy onset severe fat-soluble vitamin deficiency due to bile acid malabsorption.
Rungoe C et al.
Jpgn Reports, 2025
SLC10A2 deficiency-induced congenital chronic bile acid diarrhea and stunting.
Qie D et al.
Molecular Genetics & Genomic Medicine, 2021
Select a paper to view details