Frizzled related protein deficiency impairs muscle strength, gait and calpain 3 levels
Limb-girdle muscular dystrophy recessive 1 calpain3-related (LGMDR1), previously known as LGMD2A, is a disease caused by mutations in the CAPN3 gene. It is characterized by progressive weakness and muscle degener...
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Orphanet Journal of Rare Diseases 2020
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