Carina Wallgren‐Pettersson
University of Helsinki(FI)Folkhälsans Forskningscentrum(FI)
Publications by Year
Research Areas
Cardiomyopathy and Myosin Studies, Muscle Physiology and Disorders, Neurogenetic and Muscular Disorders Research, Cellular Mechanics and Interactions, Microtubule and mitosis dynamics
Most-Cited Works
- → Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy(2007)431 cited
- → Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy(1999)399 cited
- → Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy(1999)329 cited
- → Centronuclear (myotubular) myopathy(2008)307 cited
- → Mutations and polymorphisms of the skeletal muscle α-actin gene (ACTA1)(2009)242 cited
- → Nemaline Myopathy with Minicores Caused by Mutation of the CFL2 Gene Encoding the Skeletal Muscle Actin–Binding Protein, Cofilin-2(2006)235 cited