Novel loss of function mutations in Asian kindreds with hereditary spastic paraplegia and thin corpus callosurn (SPG11)

Những quyển sách tương tự

• Novel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafish.
  Bằng: Southgate, L, et al.
  Được phát hành: (2010)
• Clinical analysis in patients with SPG11 hereditary spastic paraplegia
  Bằng: You-Ri Kang, et al.
  Được phát hành: (2023-06-01)
• Neuropsychology and MRI correlates of neurodegeneration in SPG11 hereditary spastic paraplegia
  Bằng: Kathrin S. Utz, et al.
  Được phát hành: (2022-07-01)
• Hereditary spastic paraplegia with thin corpus callosum
  Bằng: Raina Sujeet, et al.
  Được phát hành: (2009-01-01)
• Hereditary spastic paraplegia with mental impairment, thin corpus callosum and amyotrophy: A road map to SPG11 contributors
  Bằng: Divya Goel, et al.
  Được phát hành: (2020-01-01)