Reduced <i>LYNX1</i> expression in transcriptome of human iPSC-derived neural progenitors modeling fragile X syndrome.

We found that the expression level of SLC17A6 , encoding VGLUT2, was lower in NPCs representing FXS + epilepsy phenotype when compared to FXS NPCs derived from donors without epilepsy and control NPCs at all studied time points ( Figure 5B ), but the result did not reach statistical significance when adjusted for multiple comparisons.

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