Now showing items 1-2 of 2
Long-term follow-up of R403W MYH7 and R92W TNNT2 HCM families : mutations determine left ventricular dimensions but not wall thickness during disease progression
(Clinics Cardiv Publishing, 2007-06)
The clinical profile and prognosis of patients with hypertrophic cardiomyopathy, a primary cardiac muscle disease caused mostly by mutations in sarcomeric protein-encoding genes, have been linked to particular disease-causing ...
Race and gender representation of hypertrophic cardiomyopathy or long QT syndrome cases in a South African research setting
(Clinics Cardiv Publishing, 2007-10)
We researched hypertrophic cardiomyopathy (HCM) and long QT syndrome (LQTS) as models for studying the pathophysiology of arrhythmias and hypertrophy, and in the process we have had the opportunity to compare local ...