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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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| 主要な著者: | , , , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2011
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| 主題: | |
| オンライン･アクセス: | 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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