Main findings in the study of Normand and collaborators. Early, but not late embryonic deletion of TSC1 leads to abnormal neuronal morphology and altered electrophysiological properties.

Ingo Helbig

Child Neurology Fellow and epilepsy genetics researcher at the Children’s Hospital of Philadelphia (CHOP), USA and Department of Neuropediatrics, Kiel, Germany

Facebook Twitter 

Leave a Reply

This site uses Akismet to reduce spam. Learn how your comment data is processed.