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A Novel c.3636-4 A>G Mutation in the CCDC88C Plays a Causative Role in Familial Spinocerebellar Ataxia.
Chai, Senmao; Liu, Deyang; Liu, Yajing; Sang, Ming.
Affiliation
  • Chai S; Center for Translational Medicine, Hubei Clinical Research Center of Parkinson's Disease at Xiangyang No.1 People's Hospital, Xiangyang, China, chaism16@lzu.edu.cn.
  • Liu D; Clinical Laboratory, Xian GEM Flower Changqing Hospital, Xian, China, chaism16@lzu.edu.cn.
  • Liu Y; Center for Translational Medicine, Hubei Clinical Research Center of Parkinson's Disease at Xiangyang No.1 People's Hospital, Xiangyang, China.
  • Sang M; Clinical Laboratory, Xian GEM Flower Changqing Hospital, Xian, China.
Hum Hered ; 88(1): 91-97, 2023.
Article in En | MEDLINE | ID: mdl-37899026
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spinocerebellar Degenerations / Cerebellar Ataxia / Spinocerebellar Ataxias Limits: Humans Language: En Journal: Hum Hered Year: 2023 Document type: Article Country of publication: Suiza
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spinocerebellar Degenerations / Cerebellar Ataxia / Spinocerebellar Ataxias Limits: Humans Language: En Journal: Hum Hered Year: 2023 Document type: Article Country of publication: Suiza