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A novel compound heterozygous mutation in the ACADS gene in a Chinese family with short-chain acyl-C
[会议论文] 作者：Ti-ZhenYan[1]MinZheng[2]NingTang[1]Zhe-TaoLi[1]Wu-GaoLi[1]Da-YuChen[2]BoWei[3]Shi-QiangLuo[1]Yun-ZhiLiu[3]RenCai[2,
来源：第十四次全国医学遗传学学术会议 年份：2015
Short-chain acyl-coenzyme A (CoA) dehydrogenase deficiency (SCADD) is considered a rare autosomal recessive inherited disorder of mitochondrial fatty acid b...
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