Croci, C., Traverso, M., Baratto, S. , Iacomino, M. , Pedemonte, M., Caroli, F., Scala, M., Bruno, C. and Fiorillo, C. 2022. Congenital myopathy associated with a novel mutation in MEGF10 gene, myofibrillar alteration and progressive course. Acta Myologica. 41, 3 (Sep. 2022), 111–116. DOI:https://doi.org/10.36185/2532-1900-076.