Nemaline Myopathy with Minicores Caused by Mutation of the CFL2 Gene Encoding the Skeletal Muscle Actin–Binding Protein, Cofilin-2Pankaj B. Agrawal, Alan H. Beggs, Nigel G. Laing et al.|The American Journal of Human Genetics|2006Cited by 237
Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathyJohann Böhm, Lori A.H. Erby, Valérie Biancalana et al.|Human Mutation|2012Cited by 137
The exon 55 deletion in the nebulin gene – One single founder mutation with world-wide occurrenceVilma‐Lotta Lehtokari, Carina Wallgren‐Pettersson, Rebecca S. Greenleaf et al.|Neuromuscular Disorders|2009Cited by 62