Cargando…
Paroxysmal hypnogenic dyskinesia is associated with mutations in the PRRT2 gene
OBJECTIVE: To explore the potential causative genes of paroxysmal hypnogenic dyskinesia (PHD), which was initially considered a subtype of paroxysmal dyskinesia and has been recently considered a form of nocturnal frontal lobe epilepsy (NFLE). METHODS: Eleven patients with PHD were recruited. Mutati...
Autores principales: | Liu, Xiao-Rong, Huang, Dan, Wang, Jie, Wang, Yi-Fan, Sun, Hui, Tang, Bin, Li, Wen, Lai, Jin-Xing, He, Na, Wu, Mei, Su, Tao, Meng, Heng, Shi, Yi-Wu, Li, Bing-Mei, Tang, Bei-Sha, Liao, Wei-Ping |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830198/ https://www.ncbi.nlm.nih.gov/pubmed/27123484 http://dx.doi.org/10.1212/NXG.0000000000000066 |
Ejemplares similares
-
Paroxysmal Hypnogenic Dyskinesia Responsive to Doxylamine: A Case Report
por: Williams, Daniel M.
Publicado: (2012) -
Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias
por: Wang, Jun-Ling, et al.
Publicado: (2011) -
Paroxysmal Dyskinesias in a PRRT2 Mutation Carrier
por: Marano, Massimo, et al.
Publicado: (2018) -
PRRT2 Mutations in Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions in a Taiwanese Cohort
por: Lee, Yi-Chung, et al.
Publicado: (2012) -
Novel PRRT2 mutation in an African-American family with paroxysmal kinesigenic dyskinesia
por: Hedera, Peter, et al.
Publicado: (2012)