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Primaquine-induced haemolysis in females heterozygous for G6PD deficiency
Oxidative agents can cause acute haemolytic anaemia in persons with G6PD deficiency. Understanding the relationship between G6PD genotype and the phenotypic expression of the enzyme deficiency is necessary so that severe haemolysis can be avoided. The patterns of oxidative haemolysis have been well...
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| 出版年: | Malar J |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5833093/ https://ncbi.nlm.nih.gov/pubmed/29499733 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12936-018-2248-y |
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