Mutations in dynamin 2 cause dominant centronuclear myopathyMarc Bitoun, Pascale Guicheney, Svetlana Maugenre et al.|Nature Genetics|2005Cited by 462
Distinct muscle imaging patterns in myofibrillar myopathiesDirk Fischer, Montse Olivé, Annemarie Grossmann et al.|Neurology|2008Cited by 260
Mutation Update and Genotype-Phenotype Correlations of Novel and Previously Described Mutations in<i>TPM2</i>and<i>TPM3</i>Causing Congenital MyopathiesM. Marttila, Carina Wallgren‐Pettersson, Vilma‐Lotta Lehtokari et al.|Human Mutation|2014Cited by 111
Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutationsJohann Böhm, Jocelyn Laporte, Valérie Biancalana et al.|Brain|2014Cited by 103
Quantitative analysis by polymerase chain reaction of growth hormone receptor gene expression in human liver and muscle.J-F. Martini, M C Postel-Vinay, S M Villares et al.|Endocrinology|1995Cited by 32