Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathyJohann Böhm, Lori A.H. Erby, Christopher R. Pierson et al.|Human Mutation|2012Cited by 137
Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicoresSteven E. Boyden, Peter B. Kang, Lane J. Mahoney et al.|Neurogenetics|2012Cited by 84