Read + Share

Amedeo Smart

Independent Medical Education


Read + Share

Yoo Y, Jung J, Lee YN, Lee Y, et al. GABBR2 mutations determine phenotype in Rett syndrome and epileptic encephalopathy. Ann Neurol 2017 Aug 30. doi: 10.1002/ana.25032.
PMID: 28856709


Free Medical Abstracts
Privacy Policy
Sponsors
Share
About

© Amedeo 1997-2016