Read + Share

Amedeo Smart

Independent Medical Education


Read + Share

Vardar G, Gerth F, Schmitt XJ, Rautenstrauch P, et al. Epilepsy-causing STX1B mutations translate altered protein functions into distinct phenotypes in mouse neurons. Brain 2020 Jun 23. pii: 5861027. doi: 10.1093.
PMID: 32572454


Privacy Policy