Vilma‐Lotta Lehtokari

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 · 237 citations · Full text

Medicine, Molecular Genetics, Neurology +12

Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy

Gianina Ravenscroft, Satoko Miyatake, Vilma‐Lotta Lehtokari et al. · The American Journal of Human Genetics · 2013 · 224 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy

Michaela Yuen, Sarah A. Sandaradura, James J. Dowling et al. · Journal of Clinical Investigation · 2014 · 204 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Distal myopathy caused by homozygous missense mutations in the nebulin gene

Carina Wallgren‐Pettersson, Vilma‐Lotta Lehtokari, Hannu Kalimo et al. · Brain · 2007 · 147 citations · Full text

Life Sciences, Genetics, Neurology +13

Mutation Update: The Spectra of Nebulin Variants and Associated Myopathies

Vilma‐Lotta Lehtokari, K. Kiiski, Sarah A. Sandaradura et al. · Human Mutation · 2014 · 143 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16