No abstract available
MeSH terms
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Adolescent
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Diagnosis, Differential
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Humans
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Hyperammonemia / diagnosis*
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Hyperammonemia / etiology
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Male
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Ornithine Carbamoyltransferase / genetics*
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Ornithine Carbamoyltransferase Deficiency Disease / diagnosis*
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Ornithine Carbamoyltransferase Deficiency Disease / genetics
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Point Mutation
Substances
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Ornithine Carbamoyltransferase