Impairments in contractility and cytoskeletal organisation cause nuclear defects in nemaline myopathy

Nemaline myopathy (NM) is a skeletal muscle disorder caused by mutations in genes that are generally involved in muscle contraction, in particular those related to the structure and/or regulation of the thin filament. Many pathogenic aspects of this disease remain largely unclear. Here, we report no...

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Vydáno v:Acta Neuropathol
Hlavní autoři: Ross, Jacob A., Levy, Yotam, Ripolone, Michela, Kolb, Justin S., Turmaine, Mark, Holt, Mark, Lindqvist, Johan, Claeys, Kristl G., Weis, Joachim, Monforte, Mauro, Tasca, Giorgio, Moggio, Maurizio, Figeac, Nicolas, Zammit, Peter S., Jungbluth, Heinz, Fiorillo, Chiara, Vissing, John, Witting, Nanna, Granzier, Henk, Zanoteli, Edmar, Hardeman, Edna C., Wallgren-Pettersson, Carina, Ochala, Julien
Médium: Artigo
Jazyk:Inglês
Vydáno: Springer Berlin Heidelberg 2019
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Original Paper
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6689292/
https://ncbi.nlm.nih.gov/pubmed/31218456
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00401-019-02034-8
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