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Deficiency of slow skeletal muscle troponin T causes atrophy of type I slow fibres and decreases tolerance to fatigue

The total loss of slow skeletal muscle troponin T (ssTnT encoded by TNNT1 gene) due to a nonsense mutation in codon Glu(180) causes a lethal form of recessively inherited nemaline myopathy (Amish nemaline myopathy, ANM). To investigate the pathogenesis and muscle pathophysiology of ANM, we studied t...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Wei, Bin, Lu, Yingru, Jin, J-P
Format: Artigo
Sprache:Inglês
Veröffentlicht: Blackwell publishing Ltd 2014
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3961093/
https://ncbi.nlm.nih.gov/pubmed/24445317
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/jphysiol.2013.268177
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