Pathogenesis of Autosomal Dominant Hereditary Spastic Paraplegia (SPG6) Revealed by a Rat Model

Similar Items

• High frequency of SPG4 in Taiwanese families with autosomal dominant hereditary spastic paraplegia
  od: Lan, Min-Yu, i dr.
  Izdano: (2014)
• Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11
  od: Chen, Xueping, i dr.
  Izdano: (2020)
• NIPA1 Gene Mutations Cause Autosomal Dominant Hereditary Spastic Paraplegia (SPG6)
  od: Rainier, Shirley, i dr.
  Izdano: (2003)
• Autosomal dominant hereditary spastic paraplegia: Novel mutations in the REEP1 gene (SPG31)
  od: Schlang, Katharina J, i dr.
  Izdano: (2008)
• Mutations in phospholipase DDHD2 cause autosomal recessive hereditary spastic paraplegia (SPG54)
  od: Gonzalez, Michael, i dr.
  Izdano: (2013)