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Biallelic COQ4 Variants in Hereditary Spastic Paraplegia: Clinical and Molecular Characterization.
Lin, Xiang; Jiang, Jun-Yi; Hong, Dao-Jun; Lin, Kai-Jun; Li, Jin-Jing; Chen, Yi-Jun; Qiu, Yu-Sen; Wang, Zishuai; Liao, Yi-Chu; Yang, Kang; Shi, Yan; Wang, Meng-Wen; Hsu, Shao-Lun; Hong, Shunyan; Zeng, Yi-Heng; Chen, Xiao-Chun; Wang, Ning; Lee, Yi-Chung; Chen, Wan-Jin.
Afiliación
  • Lin X; Department of Neurology, Department of Rare Diseases, Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, China.
  • Jiang JY; Department of Neurology, Department of Rare Diseases, Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, China.
  • Hong DJ; Department of Neurology, The First Affiliated Hospital of Nanchang University, Nanchang, China.
  • Lin KJ; Department of Neurology, Department of Rare Diseases, Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, China.
  • Li JJ; Department of Neurology, Department of Rare Diseases, Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, China.
  • Chen YJ; Department of Neurology, Department of Rare Diseases, Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, China.
  • Qiu YS; Department of Neurology, Department of Rare Diseases, Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, China.
  • Wang Z; Shenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, China.
  • Liao YC; Department of Neurology, Taipei Veterans General Hospital, Taipei, Taiwan.
  • Yang K; Department of Neurology, National Yang Ming Chiao Tung University, Taipei, Taiwan.
  • Shi Y; Department of Neurology, Department of Rare Diseases, Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, China.
  • Wang MW; Department of Neurology, Department of Rare Diseases, Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, China.
  • Hsu SL; Department of Neurology, Department of Rare Diseases, Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, China.
  • Hong S; Department of Neurology, Taipei Veterans General Hospital, Taipei, Taiwan.
  • Zeng YH; Department of Neurology, National Yang Ming Chiao Tung University, Taipei, Taiwan.
  • Chen XC; Department of Neurology, Department of Rare Diseases, Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, China.
  • Wang N; Department of Neurology, Department of Rare Diseases, Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, China.
  • Lee YC; Fujian Key Laboratory of Molecular Neurology, Institute of Neuroscience, Fujian Medical University, Fuzhou, China.
  • Chen WJ; Department of Neurology, Department of Rare Diseases, Institute of Neurology of First Affiliated Hospital, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, China.
Mov Disord ; 39(1): 152-163, 2024 Jan.
Article en En | MEDLINE | ID: mdl-38014483
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Pez Cebra / Paraplejía Espástica Hereditaria Límite: Animals / Humans Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: China
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Pez Cebra / Paraplejía Espástica Hereditaria Límite: Animals / Humans Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: China