GTR Home > Conditions/Phenotypes > Sarcoglycanopathies

Summary

Deficiencies or mutations in the genes for the SARCOGLYCAN COMPLEX subunits. A variety of phenotypes are associated with these mutations including a subgroup of autosomal recessive limb girdle muscular dystrophies, cardiomyopathies, and respiratory deficiency. [from MeSH]

Genes See tests for all associated and related genes

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