Argininosuccinic Aciduria in Adult : A Clinical, Electrophysiological and Biochemical Study

Author:

Grisar T.

Publisher

Springer US

Reference6 articles.

1. Allan, J. D., Cusworth, D. C., Dent, C. E., and Wilson, V. K., 1958, A disease, probably hereditary, characterized by severe mental deficient constant gross abnormality of aminoacid metabolism, Lancet 1: 182.

2. Formstecher, P., 1978, L’argininosuccinylurie, in: “Le cycle de l’urée et ses anomalies”. Paris.

3. Husquinet, H., Schoos-Barbette, S. M.Th., and Grisar, ‘T., 1981, Détection des hétérozygotes. J. Genet.Human, 29, 2, 286–295.

4. Moser, H. W., Efron, M. L., Brown, H., Diamond, R. and Neumann, G., 1967, Argininosuccinic aciduria: report of two new cases and demonstration tent elevation of blood ammonia. Amer. J. Med., 42: 9.

5. Schreier, K. and Leuchte, G., 1965, Argininbernsteinsäure, Krankheit. Dtsch. Med. Wochenschr. 90: 864.

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