Cite
MLA Citation
Hongying Ma et al.. “A PRRT2 variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with STX1B.” Epilepsia, vol. 59, 2018, pp. 1621–1630. http://access.bl.uk/ark:/81055/vdc_100066558688.0x000061