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

Slični predmeti

• Novel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafish.
  od: Southgate, L, i dr.
  Izdano: (2010)
• Clinical analysis in patients with SPG11 hereditary spastic paraplegia
  od: You-Ri Kang, i dr.
  Izdano: (2023-06-01)
• Neuropsychology and MRI correlates of neurodegeneration in SPG11 hereditary spastic paraplegia
  od: Kathrin S. Utz, i dr.
  Izdano: (2022-07-01)
• Hereditary spastic paraplegia with mental impairment, thin corpus callosum and amyotrophy: A road map to SPG11 contributors
  od: Divya Goel, i dr.
  Izdano: (2020-01-01)
• Cognitive Impairment Involving Social Cognition in SPG4 Hereditary Spastic Paraplegia
  od: Ludivine Chamard, i dr.
  Izdano: (2016-01-01)