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浏览/检索结果: 共3条，第1-3条 帮助 已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 Compound heterozygous mutations in electron transfer flavoprotein dehydrogenase identified in a young Chinese woman with late-onset glutaric aciduria type II 期刊论文 LIPIDS IN HEALTH AND DISEASE, 2017, 卷号: 16 作者:  Xue, Ying;  Zhou, Yun;  Zhang, Keqin;  Li, Ling;  Kayoumu, Abudurexiti 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/05 Glutaric aciduria type II (GA II)  Electron transfer flavoprotein dehydrogenase (ETFDH)  Autosomal recessive disorder   A novel APOC2 gene mutation identified in a Chinese patient with severe hypertriglyceridemia and recurrent pancreatitis 期刊论文 LIPIDS IN HEALTH AND DISEASE, 2016, 卷号: 15 作者:  Jiang, Jingjing;  Wang, Yuhui;  Ling, Yan;  Kayoumu, Abudurexiti;  Liu, George 收藏  |  浏览/下载：6/0  |  提交时间：2019/12/05 Hypertriglyceridemia  APOC2 gene  Mutation   A novel APOC2 gene mutation identified in a Chinese patient with severe hypertriglyceridemia and recurrent pancreatitis (vol 15, pg 12, 2016) 期刊论文 LIPIDS IN HEALTH AND DISEASE, 2016, 卷号: 15 作者:  Jiang, Jingjing;  Wang, Yuhui;  Ling, Yan;  Kayoumu, Abudurexiti;  Liu, George 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/06