ZFYVE27 (SPG33), a Novel Spastin-Binding Protein, Is Mutated in Hereditary Spastic Paraplegia

Ítems similars

• The Role of ZFYVE27/Protrudin in Hereditary Spastic Paraplegia
  per: Martignoni, Monica, et al.
  Publicat: (2008)
• Spastin gene mutation in Japanese with hereditary spastic paraplegia
  per: Yabe, I, et al.
  Publicat: (2002)
• Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia
  per: Shoukier, Moneef, et al.
  Publicat: (2009)
• Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia
  per: Shoukier, Moneef, et al.
  Publicat: (2009)
• ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis
  per: Vantaggiato, Chiara, et al.
  Publicat: (2018)