DOI:
10.1055/s-00000071
Seminars in Neurology
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References
Wang ZQ, Chen HJ, Murong SX , et al.
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.
J Mol Med (Berl) 2011;
89 (6) 569-576
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