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XB-GENEPAGE-992773
Papers associated with gabra3
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A novel GABAergic dysfunction in human Dravet syndrome., Ruffolo G, Cifelli P, Roseti C, Thom M, van Vliet EA, Limatola C, Aronica E, Palma E., Epilepsia. November 1, 2018; 59 (11): 2106-2117. |
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Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features., Niturad CE, Lev D, Kalscheuer VM, Charzewska A, Schubert J, Lerman-Sagie T, Kroes HY, Oegema R, Traverso M, Specchio N, Lassota M, Chelly J, Bennett-Back O, Carmi N, Koffler-Brill T, Iacomino M, Trivisano M, Capovilla G, Striano P, Nawara M, Rzonca S, Fischer U, Bienek M, Jensen C, Hu H, Thiele H, Altmüller J, Krause R, May P, Becker F, EuroEPINOMICS Consortium, Balling R, Biskup S, Haas SA, Nürnberg P, van Gassen KLI, Lerche H, Zara F, Maljevic S, Leshinsky-Silver E., Brain. November 1, 2017; 140 (11): 2879-2894. |
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Cloning and characterization of GABAA α subunits and GABAB subunits in Xenopus laevis during development., Kaeser GE, Rabe BA, Saha MS., Dev Dyn. April 1, 2011; 240 (4): 862-73. |
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