ArticleJournal of molecular medicine (Berlin, Germany)2011
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.
Zhi-Qiang Wang et al.PubMed ↗Publisher ↗
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