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

S. M. Houten, J. Frenkel, W. Kuis, R. J.A. Wanders, B. T. Poll-The, H. R. Waterham

Research output: Contribution to journalArticlepeer-review

20 Scopus citations
Original languageEnglish
Pages (from-to)367-370
Number of pages4
JournalJournal of Inherited Metabolic Disease
Volume23
Issue number4
DOIs
StatePublished - 2000
Externally publishedYes

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