Journal of inherited metabolic disease, 1994-01, Vol.17 (1), p.133-134
1994
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Details
- Autor(en) / Beteiligte
- Titel
- The allopurinol loading test in detecting obligate heterozygotes for OCT deficiency
- Ist Teil von
- Journal of inherited metabolic disease, 1994-01, Vol.17 (1), p.133-134
- Ort / Verlag
- Dordrecht: Kluwer Academic Publishers
- Erscheinungsjahr
- 1994
- Quelle
- SpringerLink
- Sprache
- Englisch
- Identifikatoren
- ISSN: 0141-8955eISSN: 1573-2665DOI: 10.1007/BF00735417Titel-ID: cdi_proquest_miscellaneous_76631109
- Format
- –
- Schlagworte
- Adolescent, Adult, Allopurinol, Biological and medical sciences, Chromatography, High Pressure Liquid, Errors of metabolism, Female, Genetic Carrier Screening, Humans, Medical sciences, Metabolic diseases, Middle Aged, Miscellaneous hereditary metabolic disorders, Ornithine Carbamoyltransferase - genetics, Ornithine Carbamoyltransferase Deficiency Disease, Orotic Acid - urine, Uridine - analogs & derivatives, Uridine - urine