APA

Kølvraa S., Gregersen N., Blakemore A. I., Schneidermann A. K., Winter V., Andresen B. S., Curtis D., Engel P. C., Pricille D. & Rhead W. (19911002). 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 genetics.

Chicago

Kølvraa S, Gregersen N, Blakemore A I, Schneidermann A K, Winter V, Andresen B S, Curtis D, Engel P C, Pricille D and Rhead W. 19911002. 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 genetics.

Harvard

Kølvraa S., Gregersen N., Blakemore A. I., Schneidermann A. K., Winter V., Andresen B. S., Curtis D., Engel P. C., Pricille D. and Rhead W. (19911002). 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 genetics.

MLA

Kølvraa S, Gregersen N, Blakemore A I, Schneidermann A K, Winter V, Andresen B S, Curtis D, Engel P C, Pricille D and Rhead W. 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 genetics. 19911002.