A Novel DLG1 Variant in a Family with Brugada Syndrome: Clinical Characteristics and In Silico Analysis.

Maria d'Apolito,Francesco Santoro,Rosa Santacroce,Giorgia Cordisco,Ilaria Ragnatela,Girolamo D'Arienzo,Pier Luigi Pellegrino,Natale Daniele Brunetti,Maurizio Margaglione

Genes（2023）

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摘要

A DLG1 gene variant identified was associated with BrS. The variant could modify the formation of multichannel protein complexes, affecting ion channels to specific compartments in cardiomyocytes.

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关键词

Brugada syndrome,DLG1,gene,genetics

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