Cite
HARVARD Citation
Yoo, Y. et al. (2017). GABBR2 mutations determine phenotype in rett syndrome and epileptic encephalopathy. Annals of neurology. 82 (3), pp. 466-478. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Yoo, Y. et al. (2017). GABBR2 mutations determine phenotype in rett syndrome and epileptic encephalopathy. Annals of neurology. 82 (3), pp. 466-478. [Online].