Author

Teresa Romeo Luperchio

0 works0 citationsORCID

Recent research

  • BiologyOpen access

    A patient-derived missense mouse model of Kabuki syndrome 1

    Kabuki syndrome type 1 (KS1) is a rare cause of intellectual disability resulting from heterozygous pathogenic variants in the gene encoding the histone methyltransferase KMT2D. A previously established loss-of-function mouse model of KS1 exhibits key phenotypic features, and the...

    Disease Models & Mechanisms2026-09-090 citationsDOI