Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis

Silvia Corrochano, Roope Männikkö, Peter I. Joyce, Philip McGoldrick, Jessica Wettstein, Glenda Lassi, Dipa L Raja Rayan, Gonzalo Blanco, Colin Quinn, Andrianos Liavas, Arimantas Lionikas, Neta Amior, James Dick, Estelle G. Healy, Michelle Stewart, Sarah Carter, Marie Hutchinson, Liz Bentley, Pietro Fratta, Andrea CorteseRoger Cox, Steve D. M. Brown, Valter Tucci, Henning Wackerhage, Anthony A. Amato, Linda Greensmith, Martin Koltzenburg, Michael G. Hanna, Abraham Acevedo-Arozena^*

^*Corresponding author for this work

University of York
Biology

Research output: Contribution to journal › Article › peer-review

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Finished

C2D2 research 1b - Components of a skeletal muscle z-disc mechanosensor: do they contribute to the age related decline of muscle function in humans?
Blanco, G.
1/07/12 → 31/03/13
Project: Other project › Other internal award

Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis

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C2D2 research 1b - Components of a skeletal muscle z-disc mechanosensor: do they contribute to the age related decline of muscle function in humans?