Pages that link to "Q56008646"

The following pages link to Genetic heterogeneity in Miyoshi-type distal muscular dystrophy (Q56008646):

Displaying 16 items.

• Late‐onset distal muscular dystrophy affecting the posterior calves (Q28204759) (← links)
• Characterisation of the dysferlin skeletal muscle promoter (Q28210130) (← links)
• Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies (Q33645910) (← links)
• Making sense of the limb-girdle muscular dystrophies (Q33701932) (← links)
• Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1). (Q33910216) (← links)
• A new distal myopathy with mutation in anoctamin 5. (Q34390012) (← links)
• Clinical and genetic aspects of distal myopathies (Q34464423) (← links)
• Lack of cytosolic and transmembrane domains of type XIII collagen results in progressive myopathy (Q42856204) (← links)
• Protein and gene analyses of dysferlinopathy in a large group of Japanese muscular dystrophy patients (Q44454445) (← links)
• Distal myopathies (Q44807717) (← links)
• Dysferlinopathy (LGMD2B): a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutations. (Q52141255) (← links)
• Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies) (Q57398215) (← links)
• (Q58183665) (redirect page) (← links)
• Ca-activated Cl channel TMEM16A/ANO1 identified in zebrafish skeletal muscle is crucial for action potential acceleration (Q60912767) (← links)
• Distal myopathies (Q82029893) (← links)
• Distal myopathies (Q87192794) (← links)