Case report: Coexistence of myotonia congenita and Brugada syndrome in one family

Overview of attention for article published in Frontiers in Neurology, September 2022

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RT @FrontNeurol: New Research: Case report: Coexistence of myotonia congenita and Brugada syndrome in one family: Myotonia congenita is a r…

09 Sep 2023

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Case report: Coexistence of myotonia congenita and Brugada syndrome in one family. https://t.co/ukEpy9fX9s #brugada #cardiotwitter #epeeps

11 Oct 2022

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New Research: Case report: Coexistence of myotonia congenita and Brugada syndrome in one family: Myotonia congenita is a rare neuromuscular disorder caused by CLCN1 mutations resulting in delayed muscle relaxation. Extramuscular manifestations… https://t.c

23 Sep 2022

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