Articulo
The absence of dysferlin induces the expression of functional connexin-based hemichannels in human myotubes
Fecha
2016Registro en:
1151383
WOS:000381437200006
Institución
Resumen
Background: Mutations in the gene encoding for dysferlin cause recessive autosomal muscular dystrophies called dysferlinopathies. These mutations induce several alterations in skeletal muscles, including, inflammation, increased membrane permeability and