Mevalonic aciduria: Family studies in mevalonate kinase deficiency, an inborn error of cholesterol biosynthesis

K. M. Gibson, G. Hoffmann, W. L. Nyhan, L. Sweetman, I. K. Brandt, R. S. Wappner, P. I. Bader

Research output: Contribution to journalArticlepeer-review

Original languageEnglish (US)
Pages (from-to)282-285
Number of pages4
JournalJournal of Inherited Metabolic Disease
Volume10
Issue number2 Supplement
DOIs
StatePublished - Jun 1987
Externally publishedYes

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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