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本症也是一种罕见的氨基酸先天性代谢缺陷症。在一例3个月死亡的多种畸型婴儿尿中发现两种独特的含硫氨基酸。它们是S-(2-羧丙酰)-半胱氨酸和S-(2-羧丙酰)-半酰胺。前者是异丁烯酰CoA和半胱氨
This disease is also a rare amino acid congenital metabolic defects. Two unique sulfur-containing amino acids were found in the urine of a variety of deformed infants who died at 3 months. They are S- (2-carboxypropionyl) -cysteine and S- (2-carboxypropionyl) -terminal amides. The former is methacryloyl CoA and cysteamine