The detection of molybdenum cofactor deficiency: clinical symptomatology and urinary metabolite profile.

MLA

van Gennip, A. H., et al. “The Detection of Molybdenum Cofactor Deficiency: Clinical Symptomatology and Urinary Metabolite Profile.” Journal of Inherited Metabolic Disease, vol. 17, no. 1, 1994, pp. 142–45. EBSCOhost, https://doi.org/10.1007/BF00735420.

APA

van Gennip, A. H., Abeling, N. G., Stroomer, A. E., Overmars, H., & Bakker, H. D. (1994). The detection of molybdenum cofactor deficiency: clinical symptomatology and urinary metabolite profile. Journal of Inherited Metabolic Disease, 17(1), 142–145. https://doi.org/10.1007/BF00735420

Chicago

van Gennip, A H, N G Abeling, A E Stroomer, H Overmars, and H D Bakker. 1994. “The Detection of Molybdenum Cofactor Deficiency: Clinical Symptomatology and Urinary Metabolite Profile.” Journal of Inherited Metabolic Disease 17 (1): 142–45. doi:10.1007/BF00735420.