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Whole Exome Sequencing Identifies a Novel Mutation of TPK1 in a Chinese Family with Recurrent Ataxia.
Zhu, Bizhen; Wu, Jinzhun; Chen, Guobing; Chen, Ling; Yao, Yonghua.
Affiliation
  • Zhu B; Department of Pediatrics, The First Affiliated Hospital of Xiamen University, Xiamen, 361003, China. zhubizhen@yeah.net.
  • Wu J; Department of Pediatrics, The First Affiliated Hospital of Xiamen University, Xiamen, 361003, China.
  • Chen G; Department of Pediatrics, The First Affiliated Hospital of Xiamen University, Xiamen, 361003, China.
  • Chen L; Department of Pediatrics, The First Affiliated Hospital of Xiamen University, Xiamen, 361003, China.
  • Yao Y; Department of Pediatrics, The First Affiliated Hospital of Xiamen University, Xiamen, 361003, China.
J Mol Neurosci ; 70(8): 1237-1243, 2020 Aug.
Article in En | MEDLINE | ID: mdl-32361878
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ataxia / Brain Diseases / Mutation, Missense Type of study: Prognostic_studies Limits: Child, preschool / Humans / Male Language: En Journal: J Mol Neurosci Journal subject: BIOLOGIA MOLECULAR / NEUROLOGIA Year: 2020 Document type: Article Affiliation country: Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ataxia / Brain Diseases / Mutation, Missense Type of study: Prognostic_studies Limits: Child, preschool / Humans / Male Language: En Journal: J Mol Neurosci Journal subject: BIOLOGIA MOLECULAR / NEUROLOGIA Year: 2020 Document type: Article Affiliation country: Country of publication: