中、短链酰基辅酶A脱氢酶缺乏症患儿临床特点分析及基因突变研究
An analysis of clinical characteristics and gene mutation in two patients with medium-and short-chain acyl-CoA dehydrogenase deficiency

DOI: 10.7499/j.issn.1008-8830.2016.10.021

Keywords: 脂肪酸β 氧化障碍,中链酰基辅酶A 脱氢酶,短链酰基辅酶A 脱氢酶,儿童,
Fatty acid β-oxidation disorder,Medium-chain acyl-CoA dehydrogenase,Short-chain acyl-CoA dehydrogenase,Child

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