Proteomic profiling of impaired excitation–contraction coupling and abnormal calcium handling in muscular dystrophy

The X‐linked inherited neuromuscular disorder Duchenne muscular dystrophy is characterised by primary abnormalities in the membrane cytoskeletal component dystrophin. The almost complete absence of the Dp427‐M isoform of dystrophin in skeletal muscles renders contractile fibres more susceptible to p...

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Detalles Bibliográficos
Autores principales: Dowling, Paul, Gargan, Stephen, Swandulla, Dieter, Ohlendieck, Kay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10078611/
https://www.ncbi.nlm.nih.gov/pubmed/35902360
http://dx.doi.org/10.1002/pmic.202200003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10078611/
https://www.ncbi.nlm.nih.gov/pubmed/35902360
http://dx.doi.org/10.1002/pmic.202200003

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