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

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Bibliographic Details
Published inBlood Vol. 141; no. 26; pp. 3226 - 3230
Main 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.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 29.06.2023
Subjects
Folic Acid
Humans
Mutation
Reduced Folate Carrier Protein - genetics
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Bibliography:ObjectType-Article-1
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content type line 23
ISSN:0006-4971
1528-0020
DOI:10.1182/blood.2022017968