Barely Significant
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Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).

Kidney Int · 2024 · PMC10957342 · PMID 38154558

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highly significantP < 0.0001actually significant
qPCR validation of a set of selected targets showed a highly significant correlation with the relative expression levels determined by RNA sequencing (Pearson R = 0.8955; P < 0.0001; Supplementary Figure S9 A).

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