Novel immunodeficiency caused by homozygous mutation in SLC19A1 encoding the reduced folate carrier
Shiraishi, Akira, Uygun, Vedat, Sharfe, Nigel, Beldar, Serap, Sun, Mark George Ford, Dadi, Harjit, Vong, Linda, Maxson, Michelle, Karaca, Neslihan E., Mevlitoğlu, Süleyman, Grinstein, Sergio, Artan, Reha, Merico, Daniele, Roifman, Chaim M
Published in Blood (06.02.2023)
Published in Blood (06.02.2023)
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Journal Article
Novel immunodeficiency caused by homozygous mutation in solute carrier family 19 member 1, which encodes the reduced folate carrier
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.
Published in Blood (29.06.2023)
Published in Blood (29.06.2023)
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Journal Article