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

Ítems similars

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