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Neurological outcome of patients with ornithine carbamoyltransferase deficiency
Background: Ornithine carbamoyltransferase (OCT) deficiency is the commonest of the inherited urea cycle disorders. Aims: To determine the long term neurological and cognitive outcome of continuously treated surviving patients. Methods: Twenty eight surviving children (five boys) with OCT deficiency...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
2002
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1719070/ https://ncbi.nlm.nih.gov/pubmed/11806886 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/adc.86.1.54 |
| Tagiau: |
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