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Comprehensive Mutation Scanning of LMNA in 268 Patients With Lone Atrial Fibrillation
Atrial fibrillation (AF) is a heritable, genetically heterogeneous disorder. To identify gene defects that cause or confer susceptibility to AF, a cohort of 268 unrelated patients with idiopathic forms of familial and sporadic AF was recruited. LMNA, encoding the nuclear membrane proteins, lamin A/C...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2009
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2697665/ https://ncbi.nlm.nih.gov/pubmed/19427440 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.amjcard.2009.01.354 |
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