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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שמור ב:
מידע ביבליוגרפי
הוצא לאור ב:Acta Neuropathol
Main Authors: 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
פורמט: Artigo
שפה:Inglês
יצא לאור: Springer Berlin Heidelberg 2019
נושאים:
Original Paper
גישה מקוונת: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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