1. Identification of the α-aminoadipic semialdehyde synthase which is defective in familial hyperlysinemia;Sacksteder;Am J Hum Genet,2000
2. Familial hyperlysinemias–multiple enzyme deficiencies associated with the bifunctional aminoadipic semialdehyde synthase;Cox;Trans Am Clin Climatol Assoc,1985
3. Familial hyperlysinemia: Enzyme studies, diagnostic methods, comments on terminology;Dancis;Am J Hum Genet,1979
4. Disorders of ornithine, lysine and tryptophan,” Physician's Guid. to Lab;Przyrembel;Diagnosis Metab Dis,2003
5. Laboratory guide to the methods in biochemical genetics;Blau;Lab Guid to Methods Biochem Genet,2008