Aghbolaghi AG, Lechpammer M. A rare case of centronuclear myopathy with DNM2 mutation: genotype–phenotype correlation. Autops. Case Rep. [Internet]. 2017 Jun. 30 [cited 2024 Apr. 28];7(2):43-8. Available from: https://www.revistas.usp.br/autopsy/article/view/137698