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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Podrobná bibliografie

Vydáno v:	J Clin Invest
Hlavní autoři:	Valentine, William N., Fink, Kay, Paglia, Donald E., Harris, Susan R., Adams, William S.
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	American Society for Clinical Investigation 1974
Témata:	Articles
On-line přístup:	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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