PRRT2 gene mutations in Indian paroxysmal kinesigenic dyskinesia patients

by S Prabhakara, H M Hanumantha Rao, L K Prashanth, K Anbazhagan, Rochette Jacques, Basanth Kumar Reddy
Published 2021-01-01

Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions.

by Lee, Hsien-Yang, Huang, Yong, Bruneau, Nadine, Roll, Patrice, Roberson, Elisha DO, Hermann, Mark, Quinn, Emily, Maas, James, Edwards, Robert, Ashizawa, Tetsuo, Baykan, Betul, Bhatia, Kailash, Bressman, Susan, Bruno, Michiko K, Brunt, Ewout R, Caraballo, Roberto, Echenne, Bernard, Fejerman, Natalio, Frucht, Steve, Gurnett, Christina A, Hirsch, Edouard, Houlden, Henry, Jankovic, Joseph, Lee, Wei-Ling, Lynch, David R, Mohammed, Shehla, Müller, Ulrich, Nespeca, Mark P, Renner, David, Rochette, Jacques, Rudolf, Gabrielle, Saiki, Shinji, Soong, Bing-Wen, Swoboda, Kathryn J, Tucker, Sam, Wood, Nicholas, Hanna, Michael, Bowcock, Anne M, Szepetowski, Pierre, Fu, Ying-Hui, Ptáček, Louis J
Published 2012

PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine.

by Cloarec, Robin, Bruneau, Nadine, Rudolf, Gabrielle, Massacrier, Annick, Salmi, Manal, Bataillard, Marc, Boulay, Clotilde, Caraballo, Roberto, Fejerman, Natalio, Genton, Pierre, Hirsch, Edouard, Hunter, Alasdair, Lesca, Gaetan, Motte, Jacques, Roubertie, Agathe, Sanlaville, Damien, Wong, Sau-Wei, Fu, Ying-Hui, Rochette, Jacques, Ptácek, Louis J, Szepetowski, Pierre
Published 2012