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

Blood. 2023 Jun 29;141(26):3226-3230. doi: 10.1182/blood.2022017968.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Folic Acid*
  • Humans
  • Mutation
  • Reduced Folate Carrier Protein / genetics

Substances

  • Folic Acid
  • Reduced Folate Carrier Protein