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  2. Details for: Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis.
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Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis. [electronic resource]

By:
  • Corrochano, Silvia
Contributor(s):
  • Männikkö, Roope
  • Joyce, Peter I
  • McGoldrick, Philip
  • Wettstein, Jessica
  • Lassi, Glenda
  • Raja Rayan, Dipa L
  • Blanco, Gonzalo
  • Quinn, Colin
  • Liavas, Andrianos
  • Lionikas, Arimantas
  • Amior, Neta
  • Dick, James
  • Healy, Estelle G
  • Stewart, Michelle
  • Carter, Sarah
  • Hutchinson, Marie
  • Bentley, Liz
  • Fratta, Pietro
  • Cortese, Andrea
  • Cox, Roger
  • Brown, Steve D M
  • Tucci, Valter
  • Wackerhage, Henning
  • Amato, Anthony A
  • Greensmith, Linda
  • Koltzenburg, Martin
  • Hanna, Michael G
  • Acevedo-Arozena, Abraham
Producer: 20150318Description: 3171-85 p. digitalISSN:
  • 1460-2156
Subject(s):
  • AMP-Activated Protein Kinases -- genetics
  • Animals
  • Channelopathies -- genetics
  • Humans
  • Mice
  • Mutation -- genetics
  • Myotonia -- genetics
  • Myotonic Disorders -- genetics
  • NAV1.4 Voltage-Gated Sodium Channel -- genetics
  • Paralyses, Familial Periodic -- genetics
  • Pedigree
Online resources:
  • Available from publisher's website
In: Brain : a journal of neurology vol. 137
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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

APA

Corrochano S., Männikkö R., Joyce P. I., McGoldrick P., Wettstein J., Lassi G., Raja Rayan D. L., Blanco G., Quinn C., Liavas A., Lionikas A., Amior N., Dick J., Healy E. G., Stewart M., Carter S., Hutchinson M., Bentley L., Fratta P., Cortese A., Cox R., Brown S. D. M., Tucci V., Wackerhage H., Amato A. A., Greensmith L., Koltzenburg M., Hanna M. G. & Acevedo-Arozena A. (20150318). Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis. : Brain : a journal of neurology.

Chicago

Corrochano Silvia, Männikkö Roope, Joyce Peter I, McGoldrick Philip, Wettstein Jessica, Lassi Glenda, Raja Rayan Dipa L, Blanco Gonzalo, Quinn Colin, Liavas Andrianos, Lionikas Arimantas, Amior Neta, Dick James, Healy Estelle G, Stewart Michelle, Carter Sarah, Hutchinson Marie, Bentley Liz, Fratta Pietro, Cortese Andrea, Cox Roger, Brown Steve D M, Tucci Valter, Wackerhage Henning, Amato Anthony A, Greensmith Linda, Koltzenburg Martin, Hanna Michael G and Acevedo-Arozena Abraham. 20150318. Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis. : Brain : a journal of neurology.

Harvard

Corrochano S., Männikkö R., Joyce P. I., McGoldrick P., Wettstein J., Lassi G., Raja Rayan D. L., Blanco G., Quinn C., Liavas A., Lionikas A., Amior N., Dick J., Healy E. G., Stewart M., Carter S., Hutchinson M., Bentley L., Fratta P., Cortese A., Cox R., Brown S. D. M., Tucci V., Wackerhage H., Amato A. A., Greensmith L., Koltzenburg M., Hanna M. G. and Acevedo-Arozena A. (20150318). Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis. : Brain : a journal of neurology.

MLA

Corrochano Silvia, Männikkö Roope, Joyce Peter I, McGoldrick Philip, Wettstein Jessica, Lassi Glenda, Raja Rayan Dipa L, Blanco Gonzalo, Quinn Colin, Liavas Andrianos, Lionikas Arimantas, Amior Neta, Dick James, Healy Estelle G, Stewart Michelle, Carter Sarah, Hutchinson Marie, Bentley Liz, Fratta Pietro, Cortese Andrea, Cox Roger, Brown Steve D M, Tucci Valter, Wackerhage Henning, Amato Anthony A, Greensmith Linda, Koltzenburg Martin, Hanna Michael G and Acevedo-Arozena Abraham. Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis. : Brain : a journal of neurology. 20150318.

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