1 Einträge gefunden

1. A novel missense variant in the SDR domain of the WWOX gene leads to complete loss of WWOX protein with early-onset epileptic encephalopathy and severe developmental delay

   1. Johannsen, Jessika
   2. Kortüm, Fanny
   3. Rosenberger, Georg
   4. Bokelmann, Kristin
   5. Schirmer, Markus A
   6. Denecke, Jonas
   7. Santer, René

   2018 - Forschungsinformationssystem des UKE