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  1. Jul 2024
  2. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies
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    1. scibot 13 Jul 2024
      24872

      DOI: 10.1016/j.ajhg.2023.09.009

      Resource: (BDSC Cat# 24872,RRID:BDSC_24872)

      Curator: @olekpark

      SciCrunch record: RRID:BDSC_24872

      What is this?
      DOI:10.1016/j.ajhg.2023.09.009 RRID:BDSC_24872
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    ncbi.nlm.nih.gov/pmc/articles/PMC10645550/