Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome.

Sci Rep · 2014 · PMC4206841 · PMID 25339316

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borderline significanceno p-value reported

Although the Phylop score of KCNB2 :Glu522Lys showed borderline significance, the conservation percentage was still around 80%.

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