Cite
HARVARD Citation
Bina, R. et al. (2020). De novo variants in SUPT16H cause neurodevelopmental disorders associated with corpus callosum abnormalities. Journal of medical genetics. 57 (7), pp. 461-465. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Bina, R. et al. (2020). De novo variants in SUPT16H cause neurodevelopmental disorders associated with corpus callosum abnormalities. Journal of medical genetics. 57 (7), pp. 461-465. [Online].