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The first case of a complete deficiency of diphosphoglycerate mutase in human erythrocytes.
An inherited and complete deficiency of diphosphoglycerate mutase was discovered in the erythrocytes of a 42-yr-old man of French origin whose blood hemoglobin concentration was 19.0 g/dl. Upon physical examination he was normal with the exception of a ruddy cyanosis. The morphology of his erythrocy...
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| Pubblicato in: | J Clin Invest |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
American Society for Clinical Investigation
1978
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC371847/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/152321/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI109218 |
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