Novel Mutations in the MC2R Gene in a Patient With Familial Glucocorticoid Deficiency (FGD): A Case Report and Functional Study.

Mol Genet Genomic Med · 2026 · PMC13373312 · PMID 42458748

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closest p

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highly significantno p-value reported

Statistical significance was set at * p < 0.05, while ** p < 0.01 was considered highly significant. 3.

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