William Wallefeld

Nemaline Myopathy with Minicores Caused by Mutation of the CFL2 Gene Encoding the Skeletal Muscle Actin–Binding Protein, Cofilin-2

Pankaj B. Agrawal, Rebecca S. Greenleaf, Kinga K. Tomczak et al. · The American Journal of Human Genetics · 2006 · 234 citations · Full text

Mitochondrial Myopathy, Muscle Physiology, Muscle Function +14

Novel Mutations Widen the Phenotypic Spectrum of Slow Skeletal/β-Cardiac Myosin (<i>MYH7</i>) Distal Myopathy

Phillipa J. Lamont, William Wallefeld, David Hilton‐Jones et al. · Human Mutation · 2014 · 96 citations · Full text

Cardiac Muscle, Skeletal Muscle Diseases, Genetics +24

Mutations in MYH7 cause Multi-minicore Disease (MmD) with variable cardiac involvement

Thomas Cullup, Phillipa J. Lamont, Sebahattin Çirak et al. · Neuromuscular Disorders · 2012 · 86 citations

Cardiac Muscle, Cardiomyopathy, Heart Failure +7

Abnormal actin binding of aberrant β-tropomyosins is a molecular cause of muscle weakness in <i>TPM2</i>-related nemaline and cap myopathy

M. Marttila, Elina Lemola, William Wallefeld et al. · Biochemical Journal · 2011 · 52 citations · Full text

Muscle Function, Pathology, Cytoskeleton +27

CAV3 mutations causing exercise intolerance, myalgia and rhabdomyolysis: Expanding the phenotypic spectrum of caveolinopathies

R. Scalco, A. Gardiner, Robert D. S. Pitceathly et al. · Neuromuscular Disorders · 2016 · 48 citations · Full text

Medicine, Exercise Physiology, Physiology +7