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XB-GENEPAGE-6257374
Papers associated with arhgef15
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Exome sequencing reveals new causal mutations in children with epileptic encephalopathies., Veeramah KR, Johnstone L, Karafet TM, Wolf D, Sprissler R, Salogiannis J, Barth-Maron A, Greenberg ME, Stuhlmann T, Weinert S, Jentsch TJ, Pazzi M, Restifo LL, Talwar D, Erickson RP, Hammer MF., Epilepsia. July 1, 2013; 54 (7): 1270-81. |
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