Clinical Implications and Gender Differences of KCNQ1 p.Gly168Arg Pathogenic Variant in Long QT Syndrome.

J Clin Med · 2020 · PMC7760054 · PMID 33256261

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highly significantno p-value reported

The mechanism resulting in the higher transmission rate of maternal LQTS alleles, highly significant in LQT1 families, is still unclear.

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