Congenital myopathy-causing tropomyosin mutations induce thin filament dysfunction via distinct physiological mechanisms. (Q36283381)
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English | Congenital myopathy-causing tropomyosin mutations induce thin filament dysfunction via distinct physiological mechanisms. |
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Congenital myopathy-causing tropomyosin mutations induce thin filament dysfunction via distinct physiological mechanisms (English)
David S Gokhin
Isabelle Pénisson-Besnier
Susana Quijano-Roy
Nicole Monnier
Joël Lunardi
Norma B Romero
13 July 2012
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