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 journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)367-370
Number of pages4
JournalJournal of Inherited Metabolic Disease
Publication statusPublished - 2000


  • Econometric and Statistical Methods: General
  • Genetics
  • Geneeskunde(GENK)
  • Algemeen onderzoek

Cite this