Detection of RAG mutations and prenatal diagnosis in families presenting with either T-B- severe combined immunodeficiency or Omenn's syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2004.00227.x/fullpdf
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2. The defect in murine severe combined immunodeficiency: Joining of signal sequences but not coding segments in V(D)J recombination;Lieber;Cell,1988
3. RAG mutations in human B cell-negative SCID;Schwarz;Science,1996
4. T-lymphocyte immunodeficiencies: Novel phenotypes;Fischer;Immunol Allergy Clin North Am,2000
5. Restricted heterogeneity of T lymphocytes in combined immunodeficiency with hypereosinophilia (Omenn's syndrome);De Saint Basile;J Clin Invest,1991
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