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Fig. 2 | Acta Neuropathologica Communications

Fig. 2

From: Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study

Fig. 2

Histogram showing the proportion of patients manifesting specific phenotypes. Patients are grouped based on the mutated domain; each domain is colored following the legend on the top of the figure. A. Manifestations during pregnancy or at the birth. B. Muscular manifestations. C. Osteoarticular manifestations. D. Respiratory involvement

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