MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2

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Summary

Literature (2)

Literature for OMIM 602481: MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2

Xenbase Articles:
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Na,K-ATPase mutations in familial hemiplegic migraine lead to functional inactivation., Koenderink JB,Qiu LY,Schwarz W,De Pont JJ,Friedrich T,Zifarelli G,Bamberg E, Biochim Biophys Acta. May 15, 2005; 1669(1):0006-3002.
Neurological disease mutations compromise a C-terminal ion pathway in the Na(+)/K(+)-ATPase., Poulsen H,Khandelia H,Morth JP,Bublitz M,Mouritsen OG,Egebjerg J,Nissen P, Nature. September 2, 2010; 467(7311):0143-5221.

Na,K-ATPase mutations in familial hemiplegic migraine lead to functional inactivation., Koenderink JB,Qiu LY,Schwarz W,De Pont JJ,Friedrich T,Zifarelli G,Bamberg E, Biochim Biophys Acta. May 15, 2005; 1669(1):0006-3002.

Neurological disease mutations compromise a C-terminal ion pathway in the Na(+)/K(+)-ATPase., Poulsen H,Khandelia H,Morth JP,Bublitz M,Mouritsen OG,Egebjerg J,Nissen P, Nature. September 2, 2010; 467(7311):0143-5221.