Exploring the impact of a KCNH2 missense variant on Long QT syndrome: insights into a novel gender-selective, incomplete penetrance inheritance mode

Overview of attention for article published in Frontiers in Genetics, May 2024

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Exploring the impact of a KCNH2 missense variant on Long QT syndrome: insights into a novel gender-selective, incomplete penetrance inheritance mode https://t.co/BlnimL0p1u #FrontGenet

30 May 2024

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