Cite
HARVARD Citation
Ma, H. et al. (2018). A PRRT2 variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with STX1B. Epilepsia. pp. 1621-1630. [Online].
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Ma, H. et al. (2018). A PRRT2 variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with STX1B. Epilepsia. pp. 1621-1630. [Online].