A mutation in the FBNI gene affects the conversion of profibrillin to fibrillin and is associated with skeletal features of the Marfan syndrome

DM Milewicz, J Grossfield, S-N Cao, CM Kielty, W Cevitz, T Jewett

    Research output: Contribution to journalArticlepeer-review

    Original languageEnglish
    JournalJournal of Clinical Investigation
    Volume95
    Publication statusPublished - 1995

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