Karin Y. van Spaendonck‐Zwarts

KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia

Heritability in genetic heart disease: the role of genetic background

Myofilament Remodeling and Function Is More Impaired in Peripartum Cardiomyopathy Compared with Dilated Cardiomyopathy and Ischemic Heart Disease

Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy

Genetic Analysis in 418 Index Patients with Idiopathic Dilated Cardiomyopathy: Overview of 10 Years’ Experience

Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathy

Phospholamban R14del Mutation in Patients Diagnosed with Dilated Cardiomyopathy or Arrhythmogenic Right Ventricular Cardiomyopathy: Evidence Supporting the Concept of Arrhythmogenic Cardiomyopathy