Single‐cell transcriptome analysis defines expression of Kabuki syndrome‐associated KMT2D targets and interacting partners
Objectives. Kabuki syndrome (KS) is a rare genetic disorder characterized by developmental
delay, retarded growth, and cardiac, gastrointestinal, neurocognitive, renal, craniofacial …
delay, retarded growth, and cardiac, gastrointestinal, neurocognitive, renal, craniofacial …
Manipulating Histone H3 Methylation During Development: A Caenorhabditis elegans Approach Toward Modeling Kabuki Syndrome
N Ortiz - 2020 - search.proquest.com
Sophisticated and highly coordinated mechanisms regulate histone methylation during
development. In a diseased state this can give rise to multi-organ system congenital …
development. In a diseased state this can give rise to multi-organ system congenital …