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Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function

Nemaline myopathy is characterized by muscle weakness and the presence of rod-like (nemaline) bodies. The genetic etiology of nemaline myopathy is becoming increasingly understood with mutations in ten genes now known to cause the disease. Despite this, the mechanism by which skeletal muscle weaknes...

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Détails bibliographiques
Publié dans:Acta Neuropathol
Auteurs principaux: Sztal, Tamar E., Zhao, Mo, Williams, Caitlin, Oorschot, Viola, Parslow, Adam C., Giousoh, Aminah, Yuen, Michaela, Hall, Thomas E., Costin, Adam, Ramm, Georg, Bird, Phillip I., Busch-Nentwich, Elisabeth M., Stemple, Derek L., Currie, Peter D., Cooper, Sandra T., Laing, Nigel G., Nowak, Kristen J., Bryson-Richardson, Robert J.
Format: Artigo
Langue:Inglês
Publié: Springer Berlin Heidelberg 2015
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Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4541704/
https://ncbi.nlm.nih.gov/pubmed/25931053
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00401-015-1430-3
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