MHC II deficient infant identified by newborn screening program for SCID.

Marcus, Nufar

MHC II deficient infant identified by newborn screening program for SCID. [electronic resource] - Immunologic research 08 2018 - 537-542 p. digital

Publication Type: Case Reports; Journal Article

1559-0755

10.1007/s12026-018-9019-2 doi


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