Barely Significant
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Genetic analyses of early-onset Alzheimer's disease using next generation sequencing.

Sci Rep · 2019 · PMC6557896 · PMID 31182772

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highly significantno p-value reported
Additionally, one frameshift mutation of 7 base pairs (p.Asp540fs), leading to a premature stop codon, was highly significant and should be further examined.

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