دورية أكاديمية
Mutation detection in 65 families with a possible diagnosis of ornithine carbamoyltransferase deficiency including 14 novel mutations
| العنوان: | Mutation detection in 65 families with a possible diagnosis of ornithine carbamoyltransferase deficiency including 14 novel mutations |
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| المؤلفون: | Genet, S., Cranston, T., Middleton-Price, H. R. |
| المصدر: | Journal of Inherited Metabolic Disease: Official Journal of the Society for the Study of Inborn Errors of Metabolism. November 2000 23(7):669-676 |
| 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:1005614409241 |