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Dihydropyrimidinase deficiency and congenital microvillous atrophy: Coincidence or genetic relation?

Translated title of the contribution: Dihydropyrimidinase deficiency and congenital microvillous atrophy: Coincidence or genetic relation?
  • B. Assmann
  • , G. Hoffmann
  • , L. Wagner
  • , C. Brautigam
  • , H.W. Seyberth
  • , M. Duran
  • , A.B.P. van Kuilenburg
  • , R. Wevers
  • , A.H. van Gennip

    Research output: Contribution to journal › Article › Academic › peer-review

    Translated title of the contributionDihydropyrimidinase deficiency and congenital microvillous atrophy: Coincidence or genetic relation?
    Original languageUndefined/Unknown
    Pages (from-to)681-688
    Number of pages8
    JournalJournal of Inherited Metabolic Disease
    Volume20
    Publication statusPublished - 1997

    Keywords

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

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