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Identification of Novel KMT2B Variants in Chinese Dystonia Patients via Whole-Exome Sequencing

Background: Dystonia is a movement disorder with high clinical and genetic heterogeneity. Recently mutations in lysine-specific histone methyltransferase 2B (KMT2B) gene have been reported to be associated with early-onset progressive dystonia. Methods: We performed whole-exome sequencings (WES) in...

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Detalles Bibliográficos
Autores principales:	Ma, Jun, Wang, Lin, Yang, Yingmai, Li, Shanglin, Wan, Xinhua
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2019
Materias:	Neurology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6626906/ https://www.ncbi.nlm.nih.gov/pubmed/31338059 http://dx.doi.org/10.3389/fneur.2019.00729

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