A novel IL2RG mutation associated with maternal T lymphocyte engraftment in a patient with severe combined immunodeficiency

Journal of Human Genetics

Volumn 51, Issue 5, 2006, Pages 495-497

  Kellermayer, Richard ^a   Hsu, Amy P ^b   Stankovics, József ^a   Balogh, Péter ^a   Hadzsiev, Kinga ^a   Vojcek, Ágnes ^a   Maródi, László ^c   Kajtár, Pál ^a   Kosztolányi, György ^a   Puck, Jennifer M ^b  

^a UNIVERSITY OF PÉCS   (Hungary)

^b NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^c UNIVERSITY OF DEBRECEN   (Hungary)

Author keywords

Chimerism; Engraftment; IL2RG; Maternal cells; Severe combined immunodeficiency

Indexed keywords

INTERLEUKIN 2 RECEPTOR GAMMA;

ARTICLE; CASE REPORT; COMBINED IMMUNODEFICIENCY; DISEASE ASSOCIATION; GENE MUTATION; GENETIC ASSOCIATION; GENETIC CODE; GRAFT VERSUS HOST REACTION; HETEROZYGOTE; HUMAN; INFANT; KARYOTYPE 46,XX; KARYOTYPE 46,XY; LYMPHOCYTE TRANSFUSION; MALE; MATERNAL TREATMENT;

BASE SEQUENCE; CHROMOSOMES, HUMAN, X; HUMANS; INFANT; INTERLEUKIN RECEPTOR COMMON GAMMA SUBUNIT; MALE; MOLECULAR SEQUENCE DATA; MUTATION; RECEPTORS, INTERLEUKIN; SEQUENCE ANALYSIS, DNA; SEVERE COMBINED IMMUNODEFICIENCY; T-LYMPHOCYTES;

EID: 33744968003     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10038-006-0386-5     Document Type: Article

References (6)

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