Dilated cardiomyopathy with conduction defects in a patient with partial merosin deficiency due to mutations in the laminin-α2-chain gene: A chance association or a novel phenotype?

✍ Scribed by Nicola Carboni; Giovanni Marrosu; Maurizio Porcu; Anna Mateddu; Elisabetta Solla; Eleonora Cocco; Maria A. Maioli; Valentina Oppo; Rachele Piras; Maria G. Marrosu

• Publisher: John Wiley and Sons
• Year: 2011
• Tongue: English
• Weight: 350 KB
• Volume: 44
• Category: Article
• ISSN: 0148-639X
• DOI: 10.1002/mus.22228