Barely Significant
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Analysis of the association of NPHS2 and ACTN4 genes polymorphism with nephrotic syndrome in Egyptian children.

Mol Biol Rep · 2023 · PMC10147774 · PMID 37014572

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highly significantno p-value reported
Molecular study showed a highly significant difference of NS patients from controls regarding NPHS2 rs3829795 polymorphic genotypes as the GA heterozygous genotype shows highly significant difference from controls ( P < 0.001) as well as GA + AA genotypes ( P < 0.001) in comparison with GG genotype.

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