甘油激酶缺乏症（GKD）是一种少见的X染色体隐性遗传性代谢缺陷病，可分为单纯型和复合型。
Glycerol kinase deficiency (GKD), a rare X-linked recessive disorder, is classified into two types: isolated and complex.
ATP在糖酵解的收获阶段经过两个反应生成，由磷酸甘油酸激酶和丙酮酸激酶催化。
ATP is formed in the payoff phase of glycolysis by two reactions, promoted by phosphoglycerate kinase and pyruvate kinase.
ATP在糖酵解的收获阶段经过两个反应生成，由磷酸甘油酸激酶和丙酮酸激酶催化。
ATP is formed in the payoff phase of glycolysis by two reactions, promoted by phosphoglycerate kinase and pyruvate kinase.
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