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Angelo Labate, Patrizia Tarantino, Maurizio Viri, Laura Mumoli, Monica Gagliardi, Antonino Romeo, Federico Zara, Grazia Annesi and Antonio Gambardella Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences Epilepsia 53

Article first published online: 5 NOV 2012 | DOI: 10.1111/epi.12009

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