Pages that link to "Q73061245"
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The following pages link to Optimized protein diagnosis in the autosomal recessive limb-girdle muscular dystrophies (Q73061245):
Displaying 9 items.
- From proteins to genes: immunoanalysis in the diagnosis of muscular dystrophies (Q35166268) (← links)
- Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2A (Q35753488) (← links)
- Carrier frequency of the c.525delT mutation in the SGCG gene and estimated prevalence of limb girdle muscular dystrophy type 2C among the Moroccan population (Q37687779) (← links)
- Multiplex Western blotting system for the analysis of muscular dystrophy proteins (Q42108368) (← links)
- Western blotting with diaminobenzidine detection for the diagnosis of congenital disorders of glycosylation (Q44451265) (← links)
- Revised spectrum of mutations in sarcoglycanopathies. (Q54545820) (← links)
- Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies) (Q57398215) (← links)
- Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies (Q73412938) (← links)
- Counting muscular dystrophies in the post-molecular census (Q77931827) (← links)