Novel immunodeficiency caused by homozygous mutation in solute carrier family 19 member 1, which encodes the reduced folate carrier

Shiraishi, AkiraUygun, VedatSharfe, NigelBeldar, SerapSun, Mark G. F.Dadi, HarjitVong, Linda2024-05-192024-05-1920230006-49711528-0020https://doi.org10.1182/blood.2022017968https://hdl.handle.net/20.500.12713/5912[Abstract Not Available]eninfo:eu-repo/semantics/closedAccessAcidMalabsorptionDeficiencyGeneNovel immunodeficiency caused by homozygous mutation in solute carrier family 19 member 1, which encodes the reduced folate carrierArticle141263226323036745868WOS:0011594588000012-s2.0-85150827164N/A10.1182/blood.2022017968Q1