Voltage-Dependent Sarcolemmal Ion Channel Abnormalities in the Dystrophin-Deficient Heart

Mutations in the gene encoding for the intracellular protein dystrophin cause severe forms of muscular dystrophy. These so-called dystrophinopathies are characterized by skeletal muscle weakness and degeneration. Dystrophin deficiency also gives rise to considerable complications in the heart, inclu...

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Detalles Bibliográficos
Autores principales: Koenig, Xaver, Ebner, Janine, Hilber, Karlheinz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274787/
https://www.ncbi.nlm.nih.gov/pubmed/30360568
http://dx.doi.org/10.3390/ijms19113296

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274787/
https://www.ncbi.nlm.nih.gov/pubmed/30360568
http://dx.doi.org/10.3390/ijms19113296

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