Hereditary spastic paraplegia presenting as limb dystonia with a rare SPG7 mutation

Παρόμοια τεκμήρια

• Lysosomal abnormalities in hereditary spastic paraplegia types SPG15 and SPG11
  ανά: Renvoisé, Benoît, κ.ά.
  Έκδοση: (2014)
• Multigeneration family with dominant SPG30 hereditary spastic paraplegia
  ανά: Roda, Ricardo H., κ.ά.
  Έκδοση: (2017)
• SPG3A gene polymorphisms in hereditary spastic paraplegia
  ανά: Li, Tian, κ.ά.
  Έκδοση: (2017)
• Predominant cerebellar phenotype in spastic paraplegia 7 (SPG7)
  ανά: Yahikozawa, Hiroyuki, κ.ά.
  Έκδοση: (2015)
• SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegia
  ανά: Osmanovic, Alma, κ.ά.
  Έκδοση: (2020)