The Role of TRPM4 Gene Mutations in Causing Familial Progressive Cardiac Conduction Disease: A Further Contribution

Progressive cardiac conduction disease (PCCD) is a relatively common condition in young and elderly populations, related to rare mutations in several genes, including SCN5A, SCN1B, LMNA and GJA5, TRPM4. Familial cases have also been reported. We describe a family with a large number of individuals n...

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Detalles Bibliográficos
Autores principales: Palladino, Alberto, Papa, Andrea Antonio, Petillo, Roberta, Scutifero, Marianna, Morra, Salvatore, Passamano, Luigia, Nigro, Vincenzo, Politano, Luisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871839/
https://www.ncbi.nlm.nih.gov/pubmed/35205305
http://dx.doi.org/10.3390/genes13020258

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871839/
https://www.ncbi.nlm.nih.gov/pubmed/35205305
http://dx.doi.org/10.3390/genes13020258

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