Novel immunodeficiency caused by homozygous mutation in solute carrier family 19 member 1, which encodes the reduced folate carrier.
Shiraishi A, Uygun V, Sharfe N, Beldar S, Sun MGF, Dadi H, Vong L, Maxson M, Karaca NE, Mevlitoğlu S, Grinstein S, Artan R, Merico D, Roifman CM.
Shiraishi A, et al. Among authors: uygun v.
Blood. 2023 Jun 29;141(26):3226-3230. doi: 10.1182/blood.2022017968.
Blood. 2023.
PMID: 36745868
Free article.
No abstract available.