Croci C, Traverso M, Baratto S, Iacomino M, Pedemonte M, Caroli F, Scala M, Bruno C, Fiorillo C. Congenital myopathy associated with a novel mutation in MEGF10 gene, myofibrillar alteration and progressive course. Acta Myol [Internet]. 2022 Sep. 30 [cited 2024 Nov. 21];41(3):111-6. Available from: https://www.actamyologica.it/article/view/126