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Autosomal dominant hereditary spastic paraplegia caused by mutation of UBAP1.
Wang, Jianda; Hou, Yanqi; Qi, Lina; Zhai, Shuang; Zheng, Liangwu; Han, Lin; Guo, Yufan; Zhang, Bijun; Miao, Pu; Lou, Yuting; Xu, Xiaoxiao; Wang, Ye; Ren, Yanqi; Cao, Zhenhua; Feng, Jianhua.
Afiliação
  • Wang J; Department of Pediatrics, The Second Affiliated Hospital of Zhejiang University School of Medicine, No.88 Jiefang Road, Hangzhou, 310009, Zhejiang Province, China.
  • Hou Y; RunningGene Inc., Beijing, 100083, China.
  • Qi L; Department of Pediatrics, Yuhang Branch of The Second Affiliated Hospital of Zhejiang University, Hangzhou, 330110, Zhejiang Province, China.
  • Zhai S; The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, 310052, Zhejiang Province, China.
  • Zheng L; The People's Hospital of Jiangshan, Jiangshan, 324100, Zhejiang Province, China.
  • Han L; RunningGene Inc., Beijing, 100083, China.
  • Guo Y; Department of Pediatrics, The Second Affiliated Hospital of Zhejiang University School of Medicine, No.88 Jiefang Road, Hangzhou, 310009, Zhejiang Province, China.
  • Zhang B; Department of Pediatrics, The Second Affiliated Hospital of Zhejiang University School of Medicine, No.88 Jiefang Road, Hangzhou, 310009, Zhejiang Province, China.
  • Miao P; Department of Pediatrics, The Second Affiliated Hospital of Zhejiang University School of Medicine, No.88 Jiefang Road, Hangzhou, 310009, Zhejiang Province, China.
  • Lou Y; Department of Pediatrics, The Second Affiliated Hospital of Zhejiang University School of Medicine, No.88 Jiefang Road, Hangzhou, 310009, Zhejiang Province, China.
  • Xu X; Department of Pediatrics, The Second Affiliated Hospital of Zhejiang University School of Medicine, No.88 Jiefang Road, Hangzhou, 310009, Zhejiang Province, China.
  • Wang Y; Department of Pediatrics, The Second Affiliated Hospital of Zhejiang University School of Medicine, No.88 Jiefang Road, Hangzhou, 310009, Zhejiang Province, China.
  • Ren Y; RunningGene Inc., Beijing, 100083, China.
  • Cao Z; RunningGene Inc., Beijing, 100083, China.
  • Feng J; Department of Pediatrics, The Second Affiliated Hospital of Zhejiang University School of Medicine, No.88 Jiefang Road, Hangzhou, 310009, Zhejiang Province, China. hzhz87083886@zju.edu.cn.
Neurogenetics ; 21(3): 169-177, 2020 07.
Article em En | MEDLINE | ID: mdl-32222895
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Proteínas de Transporte / Genes Dominantes / Mutação Tipo de estudo: Prognostic_studies Limite: Adolescent / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Proteínas de Transporte / Genes Dominantes / Mutação Tipo de estudo: Prognostic_studies Limite: Adolescent / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article