A new form of nucleoside phosphorylase deficiency in two brothers with defective T-cell function
Authors:
- W. Douglas BiggarWBW. Douglas Biggar
- Elosie R. GiblettEGElosie R. Giblett
- Rudolph L. OzereRORudolph L. Ozere
- B. Downey GroverBGB. Downey Grover
- 1 March 1978
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 92 (3) , 354-357
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
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- Enzyme Replacement Therapy for Adenosine Deaminase Deficiency and Severe Combined ImmunodeficiencyNew England Journal of Medicine, 1976
- An abnormal form of purine nucleoside phosphorylase in a family with a child with severe defective T-cell-and normal B-cell immunityClinica Chimica Acta, 1976
- Characterization of a cell culture model for the study of adenosine deaminase- and purine nucleoside phosphorylase-deficient immunologic diseaseCell, 1976
- Inhibition of maturation of human precursor lymphocytes by coformycin, and inhibitor of the enzyme adenosine deaminaseJournal of Experimental Medicine, 1976
- NUCLEOSIDE-PHOSPHORYLASE DEFICIENCY IN A CHILD WITH SEVERELY DEFECTIVE T-CELL IMMUNITY AND NORMAL B-CELL IMMUNITYThe Lancet, 1975
- Assignment of Nucleoside Phosphorylase to D-14 and Localization of X-linked Loci in Man by Somatic Cell GeneticsNature New Biology, 1973
- Inherited variants of human nucleoside phosphorylaseAnnals of Human Genetics, 1971
- DIFFERENTIAL SPECTROPHOTOMETRY OF PURINE COMPOUNDS BY MEANS OF SPECIFIC ENZYMESJournal of Biological Chemistry, 1947