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...

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Detalles Bibliográficos
Autores principales: Hwang, Sunhee, Mruk, Karen, Rahighi, Simin, Raub, Andrew G., Chen, Che-Hong, Dorn, Lisa E., Horikoshi, Naoki, Wakatsuki, Soichi, Chen, James K., Mochly-Rosen, Daria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6168459/
https://www.ncbi.nlm.nih.gov/pubmed/30279493
http://dx.doi.org/10.1038/s41467-018-06447-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6168459/
https://www.ncbi.nlm.nih.gov/pubmed/30279493
http://dx.doi.org/10.1038/s41467-018-06447-z

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