Article
Mutation screening of GNAL gene in patients with primary dystonia from Northeast China.
Parkinsonism & related disorders - 1 Oct 2013
Miao Jing, Wan Xin-Hua, Sun Yuan, Feng Jia-Chun, Cheng Fu-Bo
Abstract excerpt
BACKGROUND: Mutations in GNAL have recently been identified as responsible for primary dystonia, however, GNAL mutations in Chinese patients with primary dystonia are not well characterized. PATIENTS AND METHODS: Fifty-nine unrelated patients with cervical onset or cervical involved primary dystonia and 120 neurologically normal controls from Northeast China without mutations of TOR1A and THAP1 were all screened...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
