Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48)

Những quyển sách tương tự

• Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48)
  Bằng: Hirst, Jennifer, et al.
  Được phát hành: (2016)
• AP5Z1/SPG48 frequency in autosomal recessive and sporadic spastic paraplegia
  Bằng: Schlipf, Nina A, et al.
  Được phát hành: (2014)
• Interaction between AP-5 and the hereditary spastic paraplegia proteins SPG11 and SPG15
  Bằng: Hirst, Jennifer, et al.
  Được phát hành: (2013)
• SPG11 mutations are common in familial cases of complicated hereditary spastic paraplegia (HSP)
  Bằng: Paisan-Ruiz, Coro, et al.
  Được phát hành: (2008)
• Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia
  Bằng: Álvarez, Victoria, et al.
  Được phát hành: (2010)