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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...

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Detalles Bibliográficos
Autores principales:	Loges, Luiza N., Walstrom, Katherine M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Caltech Library 2021
Materias:	New Finding
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

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