Cite
HARVARD Citation
Todd, B. et al. (2018). A de novo mutation in PRICKLE1 associated with myoclonic epilepsy and autism spectrum disorder. Journal of neurogenetics. pp. 313-315. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Todd, B. et al. (2018). A de novo mutation in PRICKLE1 associated with myoclonic epilepsy and autism spectrum disorder. Journal of neurogenetics. pp. 313-315. [Online].