References
- Pompino R J, Coskun T, Demirkol Mx˙ et al. Novel mutations cause biotinidase deficiency in Turkish children. J Inherit Metab Dis. 2000; 23: 120–128
- Wolf B, Feldmann G L. The biotin dependent carboxylase deficiencies. Annu J Hum Genet 1982; 34: 699–716
- Baumgartner E R, Suormata T. Multiple carboxylase deficiency: inherited and acquired disorders of biotin metabolism. Int J Vitam Nutr Res 1977; 67: 377–384
- Wolf B. Disorders of biotin metabolism. The Metabolic and Molecular Basis of Inherited Disease (8th ed.), C R Seriver, A L Beaudet, W S Sly, D Valle. McGraw Hill, New York 2001; 3935–3960
- Cole H, Weremowicz S, Morton C C, Wolf B. Localization of serum biotinidase (BTD) to human chromosome 3 in band p25. Genomics 1994; 22: 662–663
- Niemeyer C M, Locatelli F. Chronic myeloproliferative disorders. Childhood Leukemias, C H Pui. Cambridge University Press, New York 2006; 571–598