APA

Kölker S., Christensen E., Leonard J. V., Greenberg C. R., Burlina A. B., Burlina A. P., Dixon M., Duran M., Goodman S. I., Koeller D. M., Müller E., Naughten E. R., Neumaier-Probst E., Okun J. G., Kyllerman M., Surtees R. A., Wilcken B., Hoffmann G. F. & Burgard P. (20070313). Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I). : Journal of inherited metabolic disease.

Chicago

Kölker S, Christensen E, Leonard J V, Greenberg C R, Burlina A B, Burlina A P, Dixon M, Duran M, Goodman S I, Koeller D M, Müller E, Naughten E R, Neumaier-Probst E, Okun J G, Kyllerman M, Surtees R A, Wilcken B, Hoffmann G F and Burgard P. 20070313. Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I). : Journal of inherited metabolic disease.

Harvard

Kölker S., Christensen E., Leonard J. V., Greenberg C. R., Burlina A. B., Burlina A. P., Dixon M., Duran M., Goodman S. I., Koeller D. M., Müller E., Naughten E. R., Neumaier-Probst E., Okun J. G., Kyllerman M., Surtees R. A., Wilcken B., Hoffmann G. F. and Burgard P. (20070313). Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I). : Journal of inherited metabolic disease.

MLA

Kölker S, Christensen E, Leonard J V, Greenberg C R, Burlina A B, Burlina A P, Dixon M, Duran M, Goodman S I, Koeller D M, Müller E, Naughten E R, Neumaier-Probst E, Okun J G, Kyllerman M, Surtees R A, Wilcken B, Hoffmann G F and Burgard P. Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I). : Journal of inherited metabolic disease. 20070313.