APA

Wrobe D., Henseler M., Huettler S., Pascual Pascual S. I., Chabas A. & Sandhoff K. (20000302). A non-glycosylated and functionally deficient mutant (N215H) of the sphingolipid activator protein B (SAP-B) in a novel case of metachromatic leukodystrophy (MLD). : Journal of inherited metabolic disease.

Chicago

Wrobe D, Henseler M, Huettler S, Pascual Pascual S I, Chabas A and Sandhoff K. 20000302. A non-glycosylated and functionally deficient mutant (N215H) of the sphingolipid activator protein B (SAP-B) in a novel case of metachromatic leukodystrophy (MLD). : Journal of inherited metabolic disease.

Harvard

Wrobe D., Henseler M., Huettler S., Pascual Pascual S. I., Chabas A. and Sandhoff K. (20000302). A non-glycosylated and functionally deficient mutant (N215H) of the sphingolipid activator protein B (SAP-B) in a novel case of metachromatic leukodystrophy (MLD). : Journal of inherited metabolic disease.

MLA

Wrobe D, Henseler M, Huettler S, Pascual Pascual S I, Chabas A and Sandhoff K. A non-glycosylated and functionally deficient mutant (N215H) of the sphingolipid activator protein B (SAP-B) in a novel case of metachromatic leukodystrophy (MLD). : Journal of inherited metabolic disease. 20000302.