APA
Gregersen N., Winter V. S., Corydon M. J., Corydon T. J., Rinaldo P., Ribes A., Martinez G., Bennett M. J., Vianey-Saban C., Bhala A., Hale D. E., Lehnert W., Kmoch S., Roig M., Riudor E., Eiberg H., Andresen B. S., Bross P., Bolund L. A. & Kølvraa S. (19980512). Identification of four new mutations in the short-chain acyl-CoA dehydrogenase (SCAD) gene in two patients: one of the variant alleles, 511C-->T, is present at an unexpectedly high frequency in the general population, as was the case for 625G-->A, together conferring susceptibility to ethylmalonic aciduria. : Human molecular genetics.
Chicago
Gregersen N, Winter V S, Corydon M J, Corydon T J, Rinaldo P, Ribes A, Martinez G, Bennett M J, Vianey-Saban C, Bhala A, Hale D E, Lehnert W, Kmoch S, Roig M, Riudor E, Eiberg H, Andresen B S, Bross P, Bolund L A and Kølvraa S. 19980512. Identification of four new mutations in the short-chain acyl-CoA dehydrogenase (SCAD) gene in two patients: one of the variant alleles, 511C-->T, is present at an unexpectedly high frequency in the general population, as was the case for 625G-->A, together conferring susceptibility to ethylmalonic aciduria. : Human molecular genetics.
Harvard
Gregersen N., Winter V. S., Corydon M. J., Corydon T. J., Rinaldo P., Ribes A., Martinez G., Bennett M. J., Vianey-Saban C., Bhala A., Hale D. E., Lehnert W., Kmoch S., Roig M., Riudor E., Eiberg H., Andresen B. S., Bross P., Bolund L. A. and Kølvraa S. (19980512). Identification of four new mutations in the short-chain acyl-CoA dehydrogenase (SCAD) gene in two patients: one of the variant alleles, 511C-->T, is present at an unexpectedly high frequency in the general population, as was the case for 625G-->A, together conferring susceptibility to ethylmalonic aciduria. : Human molecular genetics.
MLA
Gregersen N, Winter V S, Corydon M J, Corydon T J, Rinaldo P, Ribes A, Martinez G, Bennett M J, Vianey-Saban C, Bhala A, Hale D E, Lehnert W, Kmoch S, Roig M, Riudor E, Eiberg H, Andresen B S, Bross P, Bolund L A and Kølvraa S. Identification of four new mutations in the short-chain acyl-CoA dehydrogenase (SCAD) gene in two patients: one of the variant alleles, 511C-->T, is present at an unexpectedly high frequency in the general population, as was the case for 625G-->A, together conferring susceptibility to ethylmalonic aciduria. : Human molecular genetics. 19980512.