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Details on Person Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions
| Class:Id | LiteratureReference:936849 |
|---|---|
| _displayName | Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions |
| _timestamp | 2010-08-24 11:58:09 |
| author | [Person:936888] Vanmolkot, KR [Person:936772] Kors, EE [Person:936858] Hottenga, JJ [Person:936758] Terwindt, GM [Person:936894] Haan, J [Person:936808] Hoefnagels, WA [Person:936784] Black, DF [Person:936866] Sandkuijl, LA [Person:936793] Frants, RR [Person:936831] Ferrari, MD [Person:444143] van den Maagdenberg, AM |
| created | [InstanceEdit:936867] Jassal, Bijay, 2010-08-24 |
| journal | Ann Neurol |
| pages | 360-6 |
| pubMedIdentifier | 12953268 |
| title | Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions |
| volume | 54 |
| year | 2003 |
| (literatureReference) | [Reaction:936897] ATP1A:ATP1B:FXYD exchanges 3Na+ for 2K+ [Homo sapiens] |
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No pathways have been reviewed or authored by Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions (936849)
