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Article

Pitfalls in the detection of heterozygosity by allopurinol in a variant form of ornithine carbamoyltransferase deficiency.

Journal of inherited metabolic disease - 1 Aug 2001

Barshop B A, Nyhan W L, Climent C, Rubio V

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Share to Allopurinol
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Share to Genetic Carrier Screening

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Ornithine Carbamoyltransferase

Share to Ornithine Carbamoyltransferase Deficiency Disease

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Identifiers

PMID: 11596657
DOI: 10.1023/a:1010593916546

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