Clinical and polygraphic study of familial paroxysmal kinesigenic dyskinesia with PRRT2 mutation.
Clinical and polygraphic study of familial paroxysmal kinesigenic dyskinesia with PRRT2 mutation / Fabbri M, Marini C, Bisulli F, Di Vito L, Elia A, Guerrini R, Mei D, Tinuper P.. - In: EPILEPTIC DISORDERS. - ISSN 1294-9361. - STAMPA. - 15:(2013), pp. 123-127.
Clinical and polygraphic study of familial paroxysmal kinesigenic dyskinesia with PRRT2 mutation.
Marini C;GUERRINI, RENZO;
2013
Abstract
Clinical and polygraphic study of familial paroxysmal kinesigenic dyskinesia with PRRT2 mutation.
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