G6PD deficiency in two autochthonous Croatian families.
作者信息
Juricić D, Vince-Ribarić V, Ruzdić I, Vuletić S
出版信息
J Med Genet. 1969 Sep;6(3):281-5. doi: 10.1136/jmg.6.3.281.
Abstract
摘要
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本文引用的文献
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[Clinical contribution to the study of favism].
Lijec Vjesn. 1962 Feb;84:151-7.
2
Gene action in the X-chromosome of the mouse (Mus musculus L.).小鼠（小家鼠）X染色体上的基因作用。
Nature. 1961 Apr 22;190:372-3. doi: 10.1038/190372a0.
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An in-vitro abnormality of glutathione metabolism in erythrocytes from normal newborns: mechanism and clinical significance.正常新生儿红细胞中谷胱甘肽代谢的体外异常：机制与临床意义。
Pediatrics. 1959 Jan;23(1 Pt 1):18-32.
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Glucose-6-phosphate dehydrogenase (G6PD) deficiency, abnormal haemoglobins, and thalassaemia in Yugoslavia.南斯拉夫的葡萄糖-6-磷酸脱氢酶（G6PD）缺乏症、异常血红蛋白和地中海贫血。
J Med Genet. 1966 Mar;3(1):35-41. doi: 10.1136/jmg.3.1.35.
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