Mesh term Sarcoglycanopathies
Browse to parent terms:Cardiomyopathies
Muscular Dystrophies, Limb-Girdle
Respiration Disorders
Description
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.Search for this term in our Faculty Database
View this term at the NCBI website
