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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Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2011
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3209833/
https://ncbi.nlm.nih.gov/pubmed/21890494
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr398
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