De novo variants in CAMK2A and CAMK2B cause neurodevelopmental disorders.

Ann Clin Transl Neurol · 2018 · PMC5846454 · PMID 29560374

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did not reach statistical significanceno p-value reported

5 B), though the degrees of increase in Pro235Leu and Pro213Leu mutants did not reach statistical significance (Fig. 5 C).

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<i>De novo</i> variants in <i>CAMK2A</i> and <i>CAMK2B</i> cause neurodevelopmental disorders.

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