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sarcoglykanopatie
Subject h. sarcoglykanopatie Subject h. Sarcoglycanopathies Scope note in English 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. 
subject heading
Number of the records: 1