Diastolic dysfunction without left ventricular hypertrophy is an early finding in children with hypertrophic cardiomyopathy–causing mutations in the β-myosin heavy chain, α-tropomyosin, and myosin-binding protein C genes

✍ Scribed by Tuija Poutanen; Tero Tikanoja; Pertti Jääskeläinen; Eero Jokinen; Annuli Silvast; Markku Laakso; Johanna Kuusisto

• Book ID: 116190458
• Publisher: Elsevier Science
• Year: 2006
• Tongue: English
• Weight: 339 KB
• Volume: 151
• Category: Article
• ISSN: 1097-6744
• DOI: 10.1016/j.ahj.2005.12.005