Article
Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.
Neurology - 3 Jun 2014
Méneret Aurélie, Depienne Christel, Riant Florence, Trouillard Oriane, Bouteiller Delphine, Cincotta Massimo, Bitoun Pierre, Wickert Julia, Lagroua Isabelle, Westenberger Ana, Borgheresi Alessandra, Doummar Diane, Romano Marcello, Rossi Simone, Defebvre Luc, De Meirleir Linda, Espay Alberto J, Fiori Simona, Klebe Stephan, Quélin Chloé, Rudnik-Schöneborn Sabine, Plessis Ghislaine, Dale Russell C, Sklower Brooks Susan, Dziezyc Karolina, Pollak Pierre, Golmard Jean-Louis, Vidailhet Marie, Brice Alexis, Roze Emmanuel
Abstract excerpt
OBJECTIVE: We screened a large series of individuals with congenital mirror movements (CMM) for mutations in the 2 identified causative genes, DCC and RAD51. METHODS: We studied 6 familial and 20 simplex CMM cases. Each patient had a standardized neurologic assessment. Analysis of DCC and RAD51 c...
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