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. 1961 Dec;36(190):622–632. doi: 10.1136/adc.36.190.622

Argininosuccinic Aciduria

An Inborn Error of Amino Acid Metabolism

B Levin, Helen M M Mackay, V G Oberholzer

PMCID: PMC2012826 PMID: 14464548

622

Images in this article

Fig. 1
on p.626

Fig. 2
on p.627

Figs. 3 and 4
on p.628

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

ALLAN J. D., CUSWORTH D. C., DENT C. E., WILSON V. K. A disease, probably hereditary characterised by severe mental deficiency and a constant gross abnormality of aminoacid metabolism. Lancet. 1958 Jan 25;1(7013):182–187. doi: 10.1016/s0140-6736(58)90666-4. [DOI] [PubMed] [Google Scholar]
Bach S. J. Experiments on the metabolism of glycine. Biochem J. 1939 Jan;33(1):90–109. doi: 10.1042/bj0330090. [DOI] [PMC free article] [PubMed] [Google Scholar]
CUSWORTH D. C., DENT C. E. Renal clearances of amino acids in normal adults and in patients with aminoaciduria. Biochem J. 1960 Mar;74:550–561. doi: 10.1042/bj0740550. [DOI] [PMC free article] [PubMed] [Google Scholar]
HEILMANN J., BARROLLIER J., WATZKE E. Beitrag zur Aminosäurebestimmung auf Papierchromatogrammen. Hoppe Seylers Z Physiol Chem. 1957;309(4-6):219–220. [PubMed] [Google Scholar]
LANDING B. H. Hereditary metabolic diseases-general considerations. Metabolism. 1960 Mar;9:198–207. [PubMed] [Google Scholar]
SPORN M. B., DINGMAN W., DEFALCO A. A method for studying metabolic pathways in the brain of the intact animal; the conversion of proline to other amino acids. J Neurochem. 1959 Jun;4(2):141–147. doi: 10.1111/j.1471-4159.1959.tb13183.x. [DOI] [PubMed] [Google Scholar]
TOMLINSON S., WESTALL R. G. Argininosuccinase activity in brain tissue. Nature. 1960 Oct 15;188:235–236. doi: 10.1038/188235a0. [DOI] [PubMed] [Google Scholar]

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