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XB--6034695
Papers associated with atp1a2 (and Disease Ontology)
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A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms., Sampedro Castañeda M, Zanoteli E, Scalco RS, Scaramuzzi V, Marques Caldas V, Conti Reed U, da Silva AMS, O'Callaghan B, Phadke R, Bugiardini E, Sud R, McCall S, Hanna MG, Poulsen H, Männikkö R, Matthews E., Brain. January 1, 2018; 141 (12): 3308-3318.  |
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Na,K-ATPase mutations in familial hemiplegic migraine lead to functional inactivation., Koenderink JB, Zifarelli G, Qiu LY, Schwarz W, De Pont JJ, Bamberg E, Friedrich T., Biochim Biophys Acta. May 15, 2005; 1669 (1): 61-8. |
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