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Fig. 5 | Orphanet Journal of Rare Diseases

Fig. 5

From: MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients

Fig. 5

Morbidity map. Schematic representation of the MYH7 protein with its domain and distribution of the mutations described in the study. Most mutations are localized in the C-terminus of the protein. Near each mutation, phenotype is briefly described. DM distal myopathy; CMP cardiomyopathy; CM congenital myopathy; LGMD limb girdle muscular dystrophy; FTD fibre type disproportion

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172