| Literature DB >> 6460500 |
Abstract
A new variant of hereditary hemolytic anemia in a family due to high adenosine triphosphate (ATP) is reported. The increase in ATP levels varied from 83 to 105% in the family members. Low 2,3-diphosphoglycerate levels and low 2,3-diphosphoglyceromutase activity were observed in three family members, with normal glucose-6-phosphate dehydrogenase and pyruvate kinase activity.Entities:
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Year: 1981 PMID: 6460500 DOI: 10.1007/bf00504264
Source DB: PubMed Journal: Biochem Genet ISSN: 0006-2928 Impact factor: 1.890