Selective serotonin reuptake inhibitors ameliorate MEGF10 myopathy

MEGF10 myopathy is a rare inherited muscle disease that is named after the causative gene, MEGF10. The classic phenotype, early onset myopathy, areflexia, respiratory distress and dysphagia, is severe and immediately life-threatening. There are no disease-modifying therapies. We performed a small mo...

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Detalhes bibliográficos
Publicado no:Hum Mol Genet
Main Authors: Saha, Madhurima, Rizzo, Skylar A, Ramanathan, Manashwi, Hightower, Rylie M, Santostefano, Katherine E, Terada, Naohiro, Finkel, Richard S, Berg, Jonathan S, Chahin, Nizar, Pacak, Christina A, Wagner, Richard E, Alexander, Matthew S, Draper, Isabelle, Kang, Peter B
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2019
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General Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6606856/
https://ncbi.nlm.nih.gov/pubmed/31267131
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddz064
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