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  • Barbara Royer-Zemmour, Magali Ponsole-Lenfant, +9 authors Pierre Szepetowski
  • Biology, Medicine
  • Human molecular genetics
  • 2008 (First Published: 1 December 2008)
  • Mutations in SRPX2 (Sushi-Repeat Protein, X-linked 2) cause rolandic epilepsy with speech impairment (RESDX syndrome) or with altered development of the speech cortex (bilateral perisylvianContinue Reading