Pyrimidine metabolism in hereditary orotic aciduria

Journal of Inherited Metabolic Disease

Volumn 20, Issue 1, 1997, Pages 104-105

  Sumi, S ^a,b,d   Suchi, M ^b   Kidouchi, K ^c   Morishita, H ^b   Ohba, S ^b   Wada, Y ^b  

^a Nagoya City Child Welfare Center   (Japan)

^b NAGOYA CITY UNIV MEDICAL SCHOOL   (Japan)

^c Nagoya City Higashi General Hospital   (Japan)

^d Nagoya City Child Welfare Center   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

OROTIC ACID; PYRIMIDINE;

ACIDURIA; CASE REPORT; CHILD; FEMALE; HUMAN; PYRIMIDINE METABOLISM; REVIEW; SCHOOL CHILD;

CHILD; FOLLOW-UP STUDIES; HUMANS; OROTIC ACID; PURINE-PYRIMIDINE METABOLISM, INBORN ERRORS; PYRIMIDINES;

EID: 0031043601     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005330127995     Document Type: Review

References (3)

1. Morishita H, Kokubo M, Sumi S, et al (1986) The first case of hereditary orotic aciduria in Japan. Nipponshonikagakugakkaizasshi 90: 2775 - 2778. (In Japanese with English abstract)
2. Ohba S, Kidouchi K, Katoh T, et al (1991) Automated determination of orotic acid, uracil and pseudouridine in urine by high-performance liquid chromarography with column switching. J Chromatogr 568: 325-332.
3. Webster DR, Becroft DMO, Suttle DP (1995) Hereditary orotic aciduria and other disorders of pyrimidine metabolism. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds, The Metabolic and Molecular Bases of Inherited Disease, 7th edn. New York: McGraw-Hill, 1799 - 1837.