MHC II deficient infant identified by newborn screening program for SCID. [electronic resource]
Producer: 20190625Description: 537-542 p. digitalISSN:- 1559-0755
- CD4-Positive T-Lymphocytes -- physiology
- Chimerism
- Consanguinity
- DNA Mutational Analysis
- HLA-DR Antigens -- genetics
- Hematopoietic Stem Cell Transplantation
- Humans
- Infant, Newborn
- Israel
- Lymphopenia
- Male
- Mutation -- genetics
- Neonatal Screening
- Receptors, Antigen, T-Cell -- genetics
- Regulatory Factor X Transcription Factors -- genetics
- Severe Combined Immunodeficiency -- diagnosis
- Exome Sequencing
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Publication Type: Case Reports; Journal Article
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