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G6PD deficiency: a classic example of pharmacogenetics with on-going clinical implications
That primaquine and other drugs can trigger acute haemolytic anaemia in subjects who have an inherited mutation of the glucose 6-phosphate dehydrogenase (G6PD) gene has been known for over half a century: however, these events still occur, because when giving the drug either the G6PD status of a per...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Blackwell Publishing Ltd
2014
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153881/ https://www.ncbi.nlm.nih.gov/pubmed/24372186 http://dx.doi.org/10.1111/bjh.12665 |