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Mutation screening of GNAL gene in patients with primary dystonia from Northeast China

✍ Scribed by Miao, Jing; Wan, Xin-Hua; Sun, Yuan; Feng, Jia-Chun; Cheng, Fu-Bo


Book ID
125435618
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
358 KB
Volume
19
Category
Article
ISSN
1353-8020

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## Abstract Primary dystonias represent a clinically and genetically heterogeneous group of movement disorders. Mutations in the ϡ‐sarcoglycan (SGCE) gene have been found recently to cause myoclonus–dystonia (MD). Considerable clinical variation of SGCE mutation carriers leads to the hypothesis tha