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Molecular basis of classical mevalonic aciduria and the hyperimmunoglobulinaemia D and periodic fever syndrome: High frequency of 3 mutations in the mevalonate kinase gene

✍ Scribed by S. M. Houten; J. Frenkel; W. Kuis; R. J. A. Wanders; B. T. Poll-The; H. R. Waterham

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