1. Carson, N. A. J., Scally, B. G., Neill, D. W. and Carre, I. J. (1968). Saccharopinuria: A new inborn error of lysine metabolism.Nature,218, 679
2. Chang, Y. (1978). Lysine metabolism in the rat brain: The pipecolic acid-forming pathway.J. Neurochem.,30, 347
3. Columbo, J. P., Burgi, W., Richterich, R. and Rossi, E. (1967). Congenital lysine intolerance with periodic ammonia intoxication: A defect in L-lysine degradation.Metabolism,16, 910
4. Fischer, M. H., Gerritson, T. and Opitz, J. M. (1974). α-Aminoadipic aciduria, a non-deletarious inborn metabolic defect.Humangenetik,24, 265
5. Gatfield, P. D., Taller, E., Hinton, G. G., Wallace, A. G., Abdelnour, G. M. and Haust, M. D. (1968). Hyperpipecolatemia: A new metabolic disorder associated with neuropathy and hepatomegaly.Can. Med. Assoc. J.,99, 1215