Novel compound heterozygous mutation in <i>STAMBP</i> causes a neurodevelopmental disorder by disrupting cortical proliferation.

Front Neurosci · 2022 · PMC9399766 · PMID 36033615

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showed a trendno p-value reported

Regardless of not reaching the threshold for statistical significance, STAMBP KO organoids showed a trend of reduction in SOX2 + VZ-like regions ( Figures 4E , first row, F ).

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