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Summary Expression Gene Literature (288) GO Terms (18) Nucleotides (70) Proteins (34) Interactants (105) Wiki
XB--982766

Papers associated with scn4a (and Disease Ontology)

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Myasthenic congenital myopathy from recessive mutations at a single residue in NaV1.4., Elia N, Palmio J, Castañeda MS, Shieh PB, Quinonez M, Suominen T, Hanna MG, Männikkö R, Udd B, Cannon SC., Neurology. January 1, 2019; 92 (13): e1405-e1415.            


Stac3 enhances expression of human CaV1.1 in Xenopus oocytes and reveals gating pore currents in HypoPP mutant channels., Wu F, Quinonez M, DiFranco M, Cannon SC., J Gen Physiol. January 1, 2018; 150 (3): 475-489.                


Heterologous expression of NaV1.9 chimeras in various cell systems., Goral RO, Leipold E, Nematian-Ardestani E, Heinemann SH., Pflugers Arch. December 1, 2015; 467 (12): 2423-35.


Disrupted coupling of gating charge displacement to Na+ current activation for DIIS4 mutations in hypokalemic periodic paralysis., Mi W, Rybalchenko V, Cannon SC., J Gen Physiol. August 1, 2014; 144 (2): 137-45.        


Molecular motions of the outer ring of charge of the sodium channel: do they couple to slow inactivation?, Xiong W, Li RA, Tian Y, Tomaselli GF., J Gen Physiol. September 1, 2003; 122 (3): 323-32.            

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