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Characterization of the residual adenosine deaminating activity in the spleen of a patient with combined immunodeficiency disease and adenosine deaminase deficiency

A number of infants with an autosomal recessive form of combined immunodeficiency disease also lack adenosine deaminase (adenosine aminohydrolase; EC 3.5.4.4) activity in their erythrocytes. Other tissues from these infants contain only a few percent of the adenosine-deaminating activity present in...

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Publicat a:Proc Natl Acad Sci U S A
Autors principals: Schrader, William P., Pollara, Bernard, Meuwissen, Hilaire J.
Format: Artigo
Idioma:Inglês
Publicat: National Academy of Sciences 1978
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Accés en línia:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC411266/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/24216/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.75.1.446
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