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6-Phosphogluconolactonase deficiency, a hereditary erythrocyte enzyme deficiency: possible interaction with glucose-6-phosphate dehydrogenase deficiency.

Partial deficiency of 6-phosphogluconolactonase (EC 3.1.1.31) of the erythrocytes was discovered as an autosomal dominant disorder. Hemolytic anemia occurred in an individual who had inherited both the gene for 6-phosphogluconolactonase deficiency and that for deficiency of a nonhemolytic variant of...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Proc Natl Acad Sci U S A
Prif Awduron: Beutler, E, Kuhl, W, Gelbart, T
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: National Academy of Sciences 1985
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC397891/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3858849/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.82.11.3876
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