Acquired Glucose-6-Phosphate Dehydrogenase Deficiency

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a hereditary condition caused by mutations on chromosome X and is transmitted by a sex-linked inheritance. However, impairment of G6PD activity may result from biochemical mechanisms that are able to inhibit the enzyme in specific clinical condi...

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Detalles Bibliográficos
Autores principales: Pes, Giovanni Mario, Dore, Maria Pina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9695330/
https://www.ncbi.nlm.nih.gov/pubmed/36431166
http://dx.doi.org/10.3390/jcm11226689

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9695330/
https://www.ncbi.nlm.nih.gov/pubmed/36431166
http://dx.doi.org/10.3390/jcm11226689

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