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Mutations in PEX1 in peroxisome biogenesis disorders: G843D and a mild clinical phenotype

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Journal of Inherited Metabolic Disease

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Authors and Affiliations

  1. Department of Paediatrics, Heinrich Heine University Düsseldorf, Moorenstrasse 5, D-40225, Düsseldorf, Germany

    J. Gärtner, N. Preuss, U. Brosius & M. Biermanns

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  1. J. Gärtner
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  2. N. Preuss
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  3. U. Brosius
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  4. M. Biermanns
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Gärtner, J., Preuss, N., Brosius, U. et al. Mutations in PEX1 in peroxisome biogenesis disorders: G843D and a mild clinical phenotype. J Inherit Metab Dis 22, 311–313 (1999). https://doi.org/10.1023/A:1005599903632

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  • DOI: https://doi.org/10.1023/A:1005599903632

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