Human severe combined immunodeficiency: Genetic, phenotypic, and functional diversity in one hundred eight infants

Journal of Pediatrics

Volumn 130, Issue 3, 1997, Pages 378-387

  Buckley, R H ^a   Schiff, R I ^a   Schiff, S E ^a   Markert, M L ^a   Williams, L W ^a   Harville, T O ^a   Roberts, J L ^a   Puck, J M ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE DEAMINASE; CD16 ANTIGEN; CD20 ANTIGEN; CD3 ANTIGEN; CD4 ANTIGEN; CD8 ANTIGEN; CYTOKINE RECEPTOR; HLA ANTIGEN; IMMUNOGLOBULIN A; IMMUNOGLOBULIN E; IMMUNOGLOBULIN G; IMMUNOGLOBULIN M; PROTEIN TYROSINE KINASE;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; B LYMPHOCYTE; CARTILAGE HYPOPLASIA; COMBINED IMMUNODEFICIENCY; CONTROLLED STUDY; ENZYME DEFICIENCY; FEMALE; GENE MUTATION; GENOTYPE; HUMAN; INFANT; LYMPHOCYTE COUNT; LYMPHOCYTOPENIA; MAJOR CLINICAL STUDY; MALE; NATURAL KILLER CELL; NEWBORN; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; T LYMPHOCYTE; UNITED STATES;

EID: 0030862399     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(97)70199-9     Document Type: Article

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