Barely Significant
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Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination.

Brain · 2019 · PMC6763744 · PMID 31501903

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may be significantno p-value reported
, 2016 ), these observations may be significant and provide some explanation for the neurodevelopmental features of individuals carrying biallelic NFASC variants.

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