
Asc. Sindrome STXBP1
@stxbp1
Asociación Síndrome STXBP1. La mutación en este gen cursa con retraso cognitivo y motor, y suele presentar encefalopatía epiléptica. #ApoyoSintaxina
ID: 788356274383642624
http://www.stxbp1.es 18-10-2016 12:29:17
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Gran noticia para la familia Asc. Sindrome STXBP1 . Es un camino largo y toldos los pasos que se vayan dando suman mucho







Capsida Receives FDA Fast Track Designation for Its Potential First-in-Class IV-Administered Gene Therapy for STXBP1 Developmental and Epileptic Encephalopathy - For More Information Visit shorturl.at/sAm4f Capsida Biotherapeutics #STXBP1_DEE #Epileptic_Encephalopathy





Our census for Q2 2025 is out! 1,378 #STXBP1 patients in 57 countries. +68 patients identified in this quarter! stxbp1disorders.org/census #nopatientleftbehind #STXBP1GlobalConnect Asc. Sindrome STXBP1 stxbp1 italia Charline “STXBP1 France” STXBP1

