Mutations in L1-CAM in two families with X linked complicated spastic paraplegia, MASA syndrome, and HSAS.

Liknande verk

• MASA syndrome (a form of complicated spastic paraplegia) and X linked hydrocephalus: variable expression of the same mutation at Xq28? Call for families.
  av: Schrander-Stumpel, C, et al.
  Publicerad: (1992)
• X linked complicated spastic paraplegia, MASA syndrome, and X linked hydrocephalus owing to congenital stenosis of the aqueduct of Sylvius: variable expression of the same mutation at Xq28.
  av: Fryns, J P, et al.
  Publicerad: (1991)
• Etiological heterogeneity in X-linked spastic paraplegia.
  av: Keppen, L D, et al.
  Publicerad: (1987)
• X‐Linked Adrenoleukodystrophy Mimicking Hereditary Spastic Paraplegia
  av: Ciarlariello, Vinícius Boaratti, et al.
  Publicerad: (2019)
• MASA syndrome: new clinical features and linkage analysis using DNA probes.
  av: Schrander-Stumpel, C, et al.
  Publicerad: (1990)