The exon 55 deletion in the nebulin gene--one single founder mutation with world-wide occurrence. (33/76)

Reduced thin filament length in nebulin-knockout skeletal muscle alters isometric contractile properties. (34/76)

Mutations in the beta-myosin rod cause myosin storage myopathy via multiple mechanisms. (35/76)

Thin filament length dysregulation contributes to muscle weakness in nemaline myopathy patients with nebulin deficiency. (36/76)

alpha-Skeletal muscle actin nemaline myopathy mutants cause cell death in cultured muscle cells. (37/76)

Nemaline myopathy: clinical, histochemical and immunohistochemical features. (38/76)

Altered myofilament function depresses force generation in patients with nebulin-based nemaline myopathy (NEM2). (39/76)

Mutations of tropomyosin 3 (TPM3) are common and associated with type 1 myofiber hypotrophy in congenital fiber type disproportion. (40/76)

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