Enhanced reticulospinal output in patients with (REEP1) hereditary spastic paraplegia type 31

Lignende værker

• REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31
  af: Beetz, Christian, et al.
  Udgivet: (2008)
• Mutations in the Novel Mitochondrial Protein REEP1 Cause Hereditary Spastic Paraplegia Type 31
  af: Züchner, Stephan, et al.
  Udgivet: (2006)
• Screening for REEP1 Mutations in 31 Chinese Hereditary Spastic Paraplegia Families
  af: Ma, Xinran, et al.
  Udgivet: (2020)
• REEPing the benefits of an animal model of hereditary spastic paraplegia
  af: Deutch, Ariel Y., et al.
  Udgivet: (2013)
• Autosomal dominant hereditary spastic paraplegia: Novel mutations in the REEP1 gene (SPG31)
  af: Schlang, Katharina J, et al.
  Udgivet: (2008)