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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

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