• Familial Dilated Cardiomyopathy and Isolated Left Ventricular Noncompaction Associated With Lamin A/C Gene Mutations 

      Hermida-Prieto, Manuel; Monserrat, Lorenzo; Castro-Beiras, Alfonso; Laredo, Rafael; Soler Fernández, Rafaela; Peteiro-Vázquez, Jesús; Rodríguez, Esther; Bouzas-Zubeldia, Beatriz; Álvarez-García, Nemesio; Muñiz, Javier; Crespo-Leiro, María Generosa (Elsevier, 2004-06-23)
      [Abstract] LMNA mutations have been associated with familial or sporadic dilated cardiomyopathy (DC), with or without conduction system disease. We studied the LMNA gene in 67 consecutive patients with DC (18 had familial ...