A New Locus for Autosomal Recessive Spastic Paraplegia Associated with Mental Retardation and Distal Motor Neuropathy, SPG14, Maps to Chromosome 3q27-q28

Lignende værker

• Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11
  af: Chen, Xueping, et al.
  Udgivet: (2020)
• Mutations in phospholipase DDHD2 cause autosomal recessive hereditary spastic paraplegia (SPG54)
  af: Gonzalez, Michael, et al.
  Udgivet: (2013)
• AP5Z1/SPG48 frequency in autosomal recessive and sporadic spastic paraplegia
  af: Schlipf, Nina A, et al.
  Udgivet: (2014)
• Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1
  af: Zortea, M, et al.
  Udgivet: (2002)
• A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1–12q14
  af: Wilkinson, P, et al.
  Udgivet: (2005)