A case report of SPG11 mutations in a Chinese ARHSP-TCC family

Lignende værker

• Description of combined ARHSP/JALS phenotype in some patients with SPG11 mutations
  af: Marzieh Khani, et al.
  Udgivet: (2020-07-01)
• Description of combined ARHSP/JALS phenotype in some patients with SPG11 mutations
  af: Khani, Marzieh, et al.
  Udgivet: (2020)
• Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11
  af: Chen, Xueping, et al.
  Udgivet: (2020)
• SPG7 and Impaired Emotional Communication
  af: Zhang, Linwei, et al.
  Udgivet: (2017)
• Identification of novel compound heterozygous SPG7 mutations-related hereditary spastic paraplegia in a Chinese family: a case report
  af: Zhang, Xiaoqian, et al.
  Udgivet: (2018)