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Jul 2024
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
  
  in Public
  
  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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DOI:10.1016/j.ajhg.2023.09.009

RRID:BDSC_24872

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scibot

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ncbi.nlm.nih.gov/pmc/articles/PMC10645550/