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Correcting glucose-6-phosphate dehydrogenase deficiency with a small-molecule activator
Glucose-6-phosphate dehydrogenase (G6PD) deficiency, one of the most common human genetic enzymopathies, is caused by over 160 different point mutations and contributes to the severity of many acute and chronic diseases associated with oxidative stress, including hemolytic anemia and bilirubin-induc...
Zapisane w:
| Wydane w: | Nat Commun |
|---|---|
| Główni autorzy: | , , , , , , , , , |
| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
Nature Publishing Group UK
2018
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| Hasła przedmiotowe: | |
| Dostęp online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6168459/ https://ncbi.nlm.nih.gov/pubmed/30279493 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-018-06447-z |
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