Pages that link to "Q28241805"
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The following pages link to Early onset autosomal dominant myopathy with rigidity of the spine: a possible role for laminin beta 1? (Q28241805):
Displaying 13 items.
- Collagen VI related muscle disorders (Q24673264) (← links)
- Decreased expression of laminin beta 1 in chromosome 21-linked Bethlem myopathy (Q28139741) (← links)
- Bethlem myopathy: a slowly progressive congenital muscular dystrophy with contractures (Q28142532) (← links)
- Making sense of the limb-girdle muscular dystrophies (Q33701932) (← links)
- Immunocytochemical analysis of human muscular dystrophy (Q33840931) (← links)
- Diagnostic protein expression in human muscle biopsies (Q33891334) (← links)
- The extracellular matrix of muscle--implications for manipulation of the craniofacial musculature (Q34352280) (← links)
- Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2A (Q35753488) (← links)
- Multiplex Western blotting system for the analysis of muscular dystrophy proteins (Q42108368) (← links)
- Distribution of ten laminin chains in dystrophic and regenerating muscles (Q42479484) (← links)
- Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies) (Q57398215) (← links)
- Skeletal muscle pathology in autosomal dominant Emery-Dreifuss muscular dystrophy with lamin A/C mutations (Q57562617) (← links)
- The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach (Q73739715) (← links)