Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis-Reference-Cited by-同舟云学术

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

Published:2014-10-20 Issue:12 Volume:137 Page:3171-3185
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

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.,Acevedo-Arozena Abraham

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/137/12/3171/13799545/awu292.pdf

Reference65 articles.

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3. Inhibition of Kir2.1 (KCNJ2) by the AMP-activated protein kinase;Alesutan;Biochem Biophys Res Commun,2011

4. AMPK: a regulator of ion channels;Andersen;Commun Integr Biol,2012

5. A double mutation in families with periodic paralysis defines new aspects of sodium channel slow inactivation;Bendahhou;J Clin Invest,2000

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