The most common mutation causing medium-chain acyl-CoA dehydrogenase deficiency is strongly associated with a particular haplotype in the region of the gene
Human Genetics1991Vol. 87(4), pp. 425–8
Citations Over TimeTop 10% of 1991 papers
Steen K�lvraa, Niels Gregersen, Alexandra I. F. Blakemore, AnneK. Schneidermann, Vibeke Winter, Brage Storstein Andresen, Diana Curtis, PaulC. Engel, Divry Pricille, William J. Rhead, Lars Bolund
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