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Deletion of Transferrin Receptor 1 in Parvalbumin Interneurons Induces a Hereditary Spastic Paraplegia-Like Phenotype.
Xiong, Wenchao; Jin, Liqiang; Zhao, Yulu; Wu, Yu; Dong, Jinghua; Guo, Zhixin; Zhu, Minzhen; Dai, Yongfeng; Pan, Yida; Zhu, Xinhong.
Afiliação
  • Xiong W; School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.
  • Jin L; School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.
  • Zhao Y; School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.
  • Wu Y; School of Psychology, Shenzhen University, Shenzhen 518060, China.
  • Dong J; School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.
  • Guo Z; School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.
  • Zhu M; School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.
  • Dai Y; School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.
  • Pan Y; School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.
  • Zhu X; School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China zhuxh527@126.com.
J Neurosci ; 43(27): 5092-5113, 2023 07 05.
Article em En | MEDLINE | ID: mdl-37308296
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária Limite: Animals Idioma: En Revista: J Neurosci Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China
Texto completo
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Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária Limite: Animals Idioma: En Revista: J Neurosci Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China