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  1. Aug 2021
  2. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
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    ncbi.nlm.nih.gov/pmc/articles/PMC5963920/
  3. Jul 2021
  4. viahtml.hypothes.is viahtml.hypothes.is
    A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability
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    viahtml.hypothes.is/articles/32451