Scn5a variants as genetic arrhythmias triggers for familial bileaflet mitral valve prolapse

HIGHLIGHTS

  • who: Hager Jaouadi et al. from the Department of Cardiac Surgery, La Timone Hospital, Marseille, France have published the article: SCN5A Variants as Genetic Arrhythmias Triggers for Familial Bileaflet Mitral Valve Prolapse, in the Journal: (JOURNAL) of 21/Nov/2022
  • what: The authors report clinical and genetic investigation of family with MVP and history of syncopes and resuscitated sudden cardiac death.
  • how: In the present family study WES data were analyzed with a primary focus on genes related to MVP such as DCHS1 and DZIP1 but also on genes implicated in valvular and . . .

     

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