The role of trpm4 gene mutations in causing familial progressive cardiac conduction disease: a further contribution

HIGHLIGHTS

• who: Alberto Palladino and collaborators from the University Hospital of Campania Luigi Vanvitelli, Naples, Italy have published the research work: The Role of TRPM4 Gene Mutations in Causing Familial Progressive Cardiac Conduction Disease: A Further Contribution, in the Journal: Genes 2022, 258 of /2022/
• how: The study was conducted in accordance with the Declaration of Helsinki.

SUMMARY

Progressive cardiac conduction disorder (PCCD) is an inherited cardiac disease that may present as a primary electrical disease or in association with structural heart diseases, and often requires pacemaker (PM) implantation. The pathogenesis of . . .

 



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