Barely Significant
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A cohort of GFPT1 related congenital myasthenic syndrome in China: high frequency of c.331 c > t variant.

Orphanet J Rare Dis · 2025 · PMC12124097 · PMID 40442802

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may not be significantno p-value reported
Therefore, based on existing records, clinical differences among GFPT1-CMS patients with different variants of the same type may not be significant.

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