Development of type 1 diabetes despite severe hereditary B-cell deficiency

New England Journal of Medicine

Volumn 345, Issue 14, 2001, Pages 1036-1040

  Martin, Stephan ^a   Wolf Eichbaum, Dorothea ^b   Duinkerken, Gaby ^c   Scherbaum, Werner A ^a   Kolb, Hubert ^a   Noordzij, Jeroen G ^d   Roep, Bart O ^c  

^a HEINRICH HEINE UNIVERSITY   (Germany)

^b KLINIKUM MINDEN   (Germany)

^c LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^d ERASMUS UNIVERSITY ROTTERDAM   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOANTIBODY; BRUTON TYROSINE KINASE; C PEPTIDE; IMMUNOGLOBULIN; PROTEIN TYROSINE KINASE; UNCLASSIFIED DRUG;

ANTIBODY PRODUCTION; ARTICLE; B LYMPHOCYTE; CASE REPORT; CELL DIFFERENTIATION; CELL PROLIFERATION; DNA SEQUENCE; GENETIC RISK; HUMAN; HYPERGLYCEMIA; INSULIN BLOOD LEVEL; INSULIN DEFICIENCY; INSULIN DEPENDENT DIABETES MELLITUS; MALE; NUCLEOTIDE SEQUENCE; PHENOTYPE; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; X LINKED AGAMMAGLOBULINEMIA;

ADOLESCENT; AGAMMAGLOBULINEMIA; ANTIGENS, CD; AUTOANTIBODIES; B-LYMPHOCYTES; CELL DIVISION; CYTOKINES; DIABETES MELLITUS, TYPE 1; HUMANS; LINKAGE (GENETICS); MALE; PROTEIN-TYROSINE KINASES; SEQUENCE ANALYSIS, DNA; T-LYMPHOCYTES; X CHROMOSOME;

EID: 0035807589     PISSN: 00284793     EISSN: None     Source Type: Journal    
DOI: 10.1056/NEJMoa010465     Document Type: Article

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