| 标题 |
 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 |
| 网址 | |
| DOI | |
| 其它 |
期刊：Journal of molecular medicine (Berlin, Germany) 作者：Wang ZQ; Chen XJ; Murong SX; Wang N; Wu ZY 出版日期：2011/06/01 |
| 求助人 | |
| 下载 |
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