Combined deficiency of alpha and epsilon sarcoglycan disrupts the cardiac dystrophin complex

Cardiomyopathy is a puzzling complication in addition to skeletal muscle pathology for patients with mutations in β-, γ- or δ-sarcoglycan (SG) genes. Patients with mutations in α-SG rarely have associated cardiomyopathy, or their cardiac pathology is very mild. We hypothesize that a fifth SG, ɛ-SG,...

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Detalles Bibliográficos
Autores principales: Lancioni, Alessio, Luisa Rotundo, Ida, Monique Kobayashi, Yvonne, D'Orsi, Luca, Aurino, Stefania, Nigro, Gerardo, Piluso, Giulio, Acampora, Dario, Cacciottolo, Mafalda, Campbell, Kevin P., Nigro, Vincenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3209833/
https://www.ncbi.nlm.nih.gov/pubmed/21890494
http://dx.doi.org/10.1093/hmg/ddr398

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3209833/
https://www.ncbi.nlm.nih.gov/pubmed/21890494
http://dx.doi.org/10.1093/hmg/ddr398

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