Related Experiment Video
Updated: Mar 13, 2026

Multi-exon Skipping Using Cocktail Antisense Oligonucleotides in the Canine X-linked Muscular Dystrophy
Published on: May 24, 2016
Epidermolysis bullosa simplex with muscular dystrophy associated with PLEC deletion mutation
Valeria Carolina Alvarez1, Sini Tellervo Penttilä1, Valeria Luján Salutto1
1Instituto de Investigaciones Médicas Dr. A. Lanari (V.C.A., V.L.S., C.G.M.), Buenos Aires, Argentina; Neuromuscular Research Center (S.T.P., B.U.), Tampere University and University Hospital, Folkhälsan Genetic Institute (B.U.), and Vasa Central Hospital (B.U.), Finland.
Abstract:
Epidermolysis bullosa simplex with muscular dystrophy (EBS-MD; OMIM #226670) is an autosomal recessive disorder characterized by neonatal blistering and later-onset muscle weakness.
Related Concept Videos
Pleiotropy
Desmosomes
Satellite Stem Cells and Muscular Dystrophy
Cytoskeletal Linker Proteins - Plakins
Abnormal Proliferation
Long-patch Base Excision Repair

