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Modeling human glucose-6-phosphate dehydrogenase mutations using C. elegans GSPD-1
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked, recessive condition that causes intermittent jaundice or hemolytic anemia because of low NADPH levels in red blood cells. We performed steady-state enzyme kinetics with the recombinant C. elegans ortholog of human G6PD, GSPD-1, and...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Caltech Library
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8438584/ https://www.ncbi.nlm.nih.gov/pubmed/34532700 http://dx.doi.org/10.17912/micropub.biology.000451 |