Molecular mechanisms of riboflavin responsiveness in patients with ETF-QO variations and multiple acyl-CoA dehydrogenation deficiency
出版年份 2012 全文链接
标题
Molecular mechanisms of riboflavin responsiveness in patients with ETF-QO variations and multiple acyl-CoA dehydrogenation deficiency
作者
关键词
-
出版物
HUMAN MOLECULAR GENETICS
Volume 21, Issue 15, Pages 3435-3448
出版商
Oxford University Press (OUP)
发表日期
2012-05-20
DOI
10.1093/hmg/dds175
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Molecular analysis of 51 unrelated pedigrees with late-onset multiple acyl-CoA dehydrogenation deficiency (MADD) in southern China confirmed the most common ETFDH mutation and high carrier frequency of c.250G>A
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