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Article

Clinical outcomes and the mutation spectrum of the OTC gene in patients with ornithine transcarbamylase deficiency

21 May 2015

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 25994866
DOI: 10.1038/jhg.2015.54

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Clinical outcomes and the mutation spectrum of the OTC gene in patients with ornithine transcarbamylase deficiencyPMID 25994866Read ↗

Ten novel mutations of the ornithine transcarbamylase (OTC) gene in OTC deficiency.Semantic proximity Read ↗

Mutations and polymorphisms in the human ornithine transcarbamylase gene: mutation update addendum.Semantic proximity Read ↗

OTC gene in ornithine transcarbamylase deficiency: clinical course and mutational spectrum in seven Korean patients.Semantic proximity Read ↗

[Analysis of ornithine transcarbamylase gene mutations in three boys affected with late-onset ornithine transcarbamylase deficiency].Semantic proximity Read ↗

Genotype-Phenotype Correlations in Ornithine Transcarbamylase Deficiency: A Mutation Update.Semantic proximity Read ↗

Mutations and polymorphisms in the human ornithine transcarbamylase gene.Semantic proximity Read ↗

Mutations and polymorphisms in the human ornithine transcarbamylase (<i>OTC</i>) geneSemantic proximity Read ↗

Mutations and polymorphisms in the human ornithine transcarbamylase gene.Semantic proximity Read ↗

Phenotype and genotype analyses of ornithine transcarbamylase deficiency in Taiwanese.Semantic proximity Read ↗

[Molecular diagnosis of OTC gene mutation in a Chinese family with ornithine transcarbamylase deficiency].Semantic proximity Read ↗

Clinical and molecular characteristics of 69 Chinese patients with ornithine transcarbamylase deficiency.Semantic proximity Read ↗

An exon 1 deletion in OTC identified using chromosomal microarray analysis in a mother and her two affected deceased newborns: implications for the prenatal diagnosis of ornithine transcarbamylase deficiency.Semantic proximity Read ↗

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