1. Baumgartner, E. R., & Suormala, T. (1997). Multiple carboxylase deficiency: Inherited and acquired disorders of biotin metabolism. International Journal for Vitamin and Nutrition Research, 67, 377–384.
2. Chalmers, R. A., Mistry, J., Docherty, P. W., et al. (1994). First trimester prenatal exclusion of biotinidase deficiency. Journal of Inherited Metabolic Disease, 17, 751–752.
3. Desai, S., Ganesan, K., & Hegde, A. (2008). Biotinidase deficiency: A reversible metabolic encephalopathy. Neuroimaging and MR spectroscopic findings in a series of four patients. Pediatric Radiology, 38, 848–856.
4. Gannavarapu, S., Prasad, C., DiRaimo, J., et al. (2015). Biotinidase deficiency: Spectrum of molecular, enzymatic and clinical information from newborn screening Ontario, Canada (2007–20144). Molecular Genetics and Metabolism, 116, 146–151.
5. Gompertz, D., Draffan, G. H., Watts, J. L., et al. (1971). Biotin-responsive beta-methylcrotonylglycinuria. Lancet, 2, 22–24.