The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity.

M Gordillo, H Vega, AH Trainer, KOJ Simola

    Research output: Contribution to journalArticleScientificpeer-review

    99 Citations (Scopus)
    Original languageEnglish
    Pages (from-to)2172-2180
    JournalHuman Molecular Genetics
    Volume17
    Issue number14
    Publication statusPublished - 2008
    Publication typeA1 Journal article-refereed

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