The long quest for neonatal screening for severe combined immunodeficiency
Author:
Publisher
Elsevier BV
Subject
Immunology,Immunology and Allergy
Reference46 articles.
1. Interleukin-2 receptor gamma chain mutation results in X-linked severe combined immunodeficiency in humans;Noguchi;Cell,1993
2. Mutation of Jak3 in a patient with SCID: essential role of Jak3 in lymphoid development;Russell;Science,1995
3. Defective IL7R expression in T(-)B(+)NK(+) severe combined immunodeficiency;Puel;Nat Genet,1998
4. RAG mutations in human B cell-negative SCID;Schwarz;Science,1996
5. Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency;Moshous;Cell,2001
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