LMNA Mutation in a Family with a Strong History of Sudden Cardiac Death

We report a family with heterozygous deletion of exons 3–6 of the LMNA gene. The main presentation of affected family members was characterized by ventricular and supraventricular arrhythmias, atrioventricular (AV) block and sudden cardiac death (SCD) but also by severe dilative cardiomyopathy (DCM)...

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Detalles Bibliográficos
Autores principales: Keil, Laura, Berisha, Filip, Knappe, Dorit, Kubisch, Christian, Shoukier, Moneef, Kirchhof, Paulus, Fabritz, Larissa, Hellenbroich, Yorck, Woitschach, Rixa, Magnussen, Christina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871815/
https://www.ncbi.nlm.nih.gov/pubmed/35205214
http://dx.doi.org/10.3390/genes13020169

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871815/
https://www.ncbi.nlm.nih.gov/pubmed/35205214
http://dx.doi.org/10.3390/genes13020169

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