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APA Citation
Reinson, K., Õiglane‐Shlik, E., Talvik, I., Vaher, U., Õunapuu, A., Ennok, M., Teek, R., Pajusalu, S., Murumets, Ü., Tomberg, T., Puusepp, S., Piirsoo, A., Reimand, T., & Õunap, K. (2016). biallelic CACNA1A mutations cause early onset epileptic encephalopathy with progressive cerebral, cerebellar, and optic nerve atrophy. American journal of medical genetics, 170(8), 2173–2176. http://access.bl.uk/ark:/81055/vdc_100034681256.0x000017