Congenital mirror movements: Mutational analysis of RAD51 and DCC in 26 cases

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 codi...

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Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Lippincott Williams & Wilkins 2014
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4105259/
https://ncbi.nlm.nih.gov/pubmed/24808016
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000000477
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