Novel immunodeficiency caused by homozygous mutation in solute carrier family 19 member 1, which encodes the reduced folate carrier
- Resource Type
- Short Communication
- Authors
- Shiraishi, Akira; Uygun, Vedat; Sharfe, Nigel; Beldar, Serap; Sun, Mark G. F.; Dadi, Harjit; Vong, Linda; Maxson, Michelle; Karaca, Neslihan E.; Mevlitoğlu, Süleyman; Grinstein, Sergio; Artan, Reha; Merico, Daniele; Roifman, Chaim M.
- Source
- In Blood 29 June 2023 141(26):3226-3230
- Subject
- Immunobiology and Immunotherapy
- Language
- ISSN
- 0006-4971