Novel immunodeficiency caused by homozygous mutation in solute carrier family 19 member 1, which encodes the reduced folate carrierAkira Shiraishi,Vedat Uygun,Nigel Sharfe,Serap Beldar,Mark G. F. Sun,Harjit Dadi,Linda Vong,Michelle Maxson,Neslihan E. Karaca,Sueleyman Mevlitoglu,Sergio Grinstein,Reha Artan,Daniele Merico,Chaim M. RoifmanBlood（2023）引用 0|浏览33暂无评分AI 理解论文溯源树样例生成溯源树，研究论文发展脉络Chat Paper正在生成论文摘要
