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

Ижил төстэй зүйлс

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