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Article

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: high frequency of the G1528C mutation with no apparent correlation with the clinical phenotype.

Journal of inherited metabolic disease - 1 Jan 1995

Ijlst L, Uskikubo S, Kamijo T, Hashimoto T, Ruiter J P, de Klerk J B, Wanders R J

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Share to 3-Hydroxyacyl CoA Dehydrogenases
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 7564258
DOI: 10.1007/BF00711778

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