Congenital anomalies in glutaric aciduria type 2.
作者信息
Mitchell G, Saudubray J M, Gubler M C, Habib R, Ogier H, Frezal J, Boue J
出版信息
J Pediatr. 1984 Jun;104(6):961-2. doi: 10.1016/s0022-3476(84)80520-x.
PMID:6726538
Abstract
摘要
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引用本文的文献
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The multiple acyl-coenzyme A dehydrogenation disorders, glutaric aciduria type II and ethylmalonic-adipic aciduria. Mitochondrial fatty acid oxidation, acyl-coenzyme A dehydrogenase, and electron transfer flavoprotein activities in fibroblasts.多种酰基辅酶A脱氢酶缺乏症，即II型戊二酸尿症和乙基丙二酸-己二酸尿症。成纤维细胞中的线粒体脂肪酸氧化、酰基辅酶A脱氢酶及电子传递黄素蛋白活性。
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