Heterogeneity of phenotype in two siblings with adenosine deaminase deficiency
- 28 February 1994
- journal article
- case report
- Published by Elsevier in Journal of Allergy and Clinical Immunology
- Vol. 93 (2) , 543-550
- https://doi.org/10.1016/0091-6749(94)90365-4
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Atomic Structure of Adenosine Deaminase Complexed with a Transition-State Analog: Understanding Catalysis and Immunodeficiency MutationsScience, 1991
- Human antibody responses to bacteriophage φX 174: Sequential induction of IgM and IgG subclass antibodyClinical Immunology and Immunopathology, 1989
- Adenosine deaminase deficiency with late onset of recurrent infections: Response to treatment with polyethylene glycol-modified adenosine deaminaseThe Journal of Pediatrics, 1988
- Adenosine deaminase (ADA) deficiency due to deletion of the ADA gene promoter and first exon by homologous recombination between two Alu elements.Journal of Clinical Investigation, 1988
- Adenosine deaminase and purine nucleoside phosphorylase deficiencies: Evaluation of therapeutic interventions in eight patientsJournal of Clinical Immunology, 1987
- Treatment of Adenosine Deaminase Deficiency with Polyethylene Glycol–Modified Adenosine DeaminaseNew England Journal of Medicine, 1987
- Identification of a point mutation in the adenosine deaminase gene responsible for immunodeficiency.Journal of Clinical Investigation, 1985
- Erythrocyte Adenosine Deaminase Deficiency without ImmunodeficiencyJournal of Clinical Investigation, 1979
- In Vivo and in Vitro Effects of Thymosin and Adenosine Deaminase on Adenosine-Deaminase-Deficient LymphocytesNew England Journal of Medicine, 1979
- ADENOSINE-DEAMINASE DEFICIENCY IN A CHILD DIAGNOSED PRENATALLYThe Lancet, 1975