No abstract available
MeSH terms
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Amino Acid Metabolism, Inborn Errors* / etiology
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Amino Acid Metabolism, Inborn Errors* / physiopathology
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Humans
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Mutation
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Ornithine Carbamoyltransferase / genetics
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Ornithine Carbamoyltransferase Deficiency Disease*
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Prognosis
Substances
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Ornithine Carbamoyltransferase