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Not Just Loss-of-Function Variations: Identification of a Hypermorphic Variant in a Patient With a CDKL5 Missense Substitution.

Neurol Genet · 2022 · PMC8906656 · PMID 35280940

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Furthermore, normalization of the CDKL5 signal to the cotransfected RFP showed a tendency toward increased protein levels of the mutant CDKL5, although it did not reach statistical significance ( Figure 3, A and E ).

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