Publication | Closed Access
A novel γ-sarcoglycan mutation causing childhood onset, slowly progressive limb girdle muscular dystrophy
24
Citations
17
References
1998
Year
Rare DiseasesMendelian DisorderGenetic DisorderMedicinePathologyDegenerative DiseaseChildhood OnsetNeuromuscular PathologyCell BiologyNovel γ-Sarcoglycan Mutation
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