Figure 4From: Genotype-phenotype correlations in recessive RYR1-related myopathiesAssessment of associations with ophthalmoparesis. (A) Ophthalmoparesis among hispathologic diagnosis. Abbreviations: multimincore disease (MmD), centronuclear myopathy (CNM), RYR1-related myopathy (RRM), congenital fiber type disproportion (CFTD). (B) Ophthalmoparesis among mutation types.Back to article page