Barely Significant
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In a cohort of 961 clinically suspected Duchenne muscular dystrophy patients, 105 were diagnosed to have other muscular dystrophies (OMDs), with LGMD2E (variant SGCB c.544A>C) being the most common.

Mol Genet Genomic Med · 2024 · PMC11568062 · PMID 39548682

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may be significantno p-value reported
A word of caution: while the contribution of one or more variants to the muscular dystrophies described may be significant, it is not possible to draw any conclusions about the contributions of these mutant genes with regard to disease causation at this time. 3.8.

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