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Article

Diagnosis of ornithine transcarbamylase deficiency secondary to p.Leu301Phe mutation in an adult patient.

Revue neurologique - 1 Mar 2012

Morel N, Corne C, Aquaviva C, Besson G

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Share to Early Diagnosis
Share to Amino Acid Substitution
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Ornithine Carbamoyltransferase Deficiency Disease

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PMID: 22340867
DOI: 10.1016/j.neurol.2011.06.008

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Diagnosis of ornithine transcarbamylase deficiency secondary to p.Leu301Phe mutation in an adult patient.PMID 22340867Read ↗

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