Barely Significant
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A comprehensive update of genotype-phenotype correlations in PMM2-CDG: insights from molecular and structural analyses.

Orphanet J Rare Dis · 2025 · PMC12042452 · PMID 40307862

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highly significantno p-value reported
This type of correlation could be highly significant in determining disease progression, prognosis, severity and in developing genome-personalized therapies.

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