Hereditary Hemolytic Anemia with Human Erythrocyte Pyrimidine 5′-Nucleotidase Deficiency

A severe deficiency of a red cell pyrimidine 5′-nucleotidase was found to be associated with hereditary hemolytic anemia in four members of three kindreds. The syndrome was characterized by marked increases above normal in red cell basophilic stippling, total nucleotides, and GSH and by a fairly sev...

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Détails bibliographiques

Publié dans:	J Clin Invest
Auteurs principaux:	Valentine, William N., Fink, Kay, Paglia, Donald E., Harris, Susan R., Adams, William S.
Format:	Artigo
Langue:	Inglês
Publié:	American Society for Clinical Investigation 1974
Sujets:	Articles
Accès en ligne:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC301626/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/4372252/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI107826
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