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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Dades bibliogràfiques
Publicat a:Open Heart
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: BMJ Publishing Group 2017
Matèries:
Heart Failure and Cardiomyopathies
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5255551/
https://ncbi.nlm.nih.gov/pubmed/28123761
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/openhrt-2016-000474
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