The most common mutation causing medium-chain acyl-CoA dehydrogenase deficiency is strongly associated with a particular haplotype in the region of the gene
Steen K�lvraa(Aarhus University), Lars Bolund(BGI Group (China)), Divry Pricille(Hôpital Debrousse), AnneK. Schneidermann(Aarhus University), Alexandra I. F. Blakemore(Imperial College London), William J. Rhead(Children's Hospital of Wisconsin), Diana Curtis(University of Sheffield), PaulC. Engel(University of Sheffield), Niels Gregersen(Technical University of Denmark), Vibeke Winter(Aarhus University), Brage Storstein Andresen(University of Southern Denmark)
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