Clinical disease presentation and ECG characteristics of LMNA mutation carriers

OBJECTIVE: Mutations in the LMNA gene encoding lamins A and C of the nuclear lamina are a frequent cause of cardiomyopathy accounting for 5–8% of familial dilated cardiomyopathy (DCM). Our aim was to study disease onset, presentation and progression among LMNA mutation carriers. METHODS: Clinical fo...

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Detalles Bibliográficos
Autores principales: Ollila, Laura, Nikus, Kjell, Holmström, Miia, Jalanko, Mikko, Jurkko, Raija, Kaartinen, Maija, Koskenvuo, Juha, Kuusisto, Johanna, Kärkkäinen, Satu, Palojoki, Eeva, Reissell, Eeva, Piirilä, Päivi, Heliö, Tiina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2017
Materias:
Heart Failure and Cardiomyopathies
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5255551/
https://www.ncbi.nlm.nih.gov/pubmed/28123761
http://dx.doi.org/10.1136/openhrt-2016-000474

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5255551/
https://www.ncbi.nlm.nih.gov/pubmed/28123761
http://dx.doi.org/10.1136/openhrt-2016-000474

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