An αtropomyosin mutation alters dimer preference in nemaline myopathy

Nemaline myopathy is a human neuromuscular disorder associated with muscle weakness, Z‐line accumulations (rods), and myofibrillar disorganization. Disease‐causing mutations have been identified in genes encoding muscle thin filament proteins: actin, nebulin, slow troponin T, βTropomyosin, and αTrop...

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Veröffentlicht in:	Annals of neurology 2005-01, Vol.57 (1), p.42-49
Hauptverfasser:	Corbett, Mark A., Anthony Akkari, P., Domazetovska, Ana, Cooper, Sandra T., North, Kathryn N., Laing, Nigel G., Gunning, Peter W., Hardeman, Edna C.
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Diseases of striated muscles. Neuromuscular diseases Medical sciences Neurology
Online-Zugang:	Volltext
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