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Molecular abnormality of phosphoglycerate kinase-Uppsala associated with chronic nonspherocytic hemolytic anemia.

Inherited deficiency of phosphoglycerate kinase (PGK; ATP:3-phosphoglycerate 1-phosphotransferase, EC 2.7.2.3) is associated with chronic nonspherocytic hemolytic anemia and mental disorders in man. One such variant, PGK-Uppsala, was purified to homogeneity. PGK-Uppsala had a lower-than-normal speci...

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Bibliografski detalji
Glavni autori: Fujii, H, Yoshida, A
Format: Artigo
Jezik:Inglês
Izdano: 1980
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC350080/
https://ncbi.nlm.nih.gov/pubmed/6933565
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