دورية أكاديمية
SHORT REPORT: Pitfalls in the detection of heterozygosity by allopurinol in a variant form of ornithine carbamoyltransferase deficiency
| العنوان: | SHORT REPORT: Pitfalls in the detection of heterozygosity by allopurinol in a variant form of ornithine carbamoyltransferase deficiency |
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| المؤلفون: | Barshop, B. A., Nyhan, W. L., Climent, C., Rubio, V. |
| المصدر: | Journal of Inherited Metabolic Disease: Official Journal of the Society for the Study of Inborn Errors of Metabolism. July 2001 24(4):513-514 |
| قاعدة البيانات: | Springer Nature Journals |
Find this article in full text from Springer Verlag. 
Full Text Finder | تدمد: | 01418955 15732665 |
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| DOI: | 10.1023/a:1010593916546 |