Pathogenic Variant of REEP1 in a Korean Family with Autosomal-Dominant Hereditary Spastic Paraplegia

Ítems similars

• Autosomal dominant hereditary spastic paraplegia: Novel mutations in the REEP1 gene (SPG31)
  per: Schlang, Katharina J, et al.
  Publicat: (2008)
• Mutation analysis of SPAST, ATL1, and REEP1 in Korean Patients with Hereditary Spastic Paraplegia
  per: Kim, Tae-Hyoung, et al.
  Publicat: (2014)
• Erratum: Mutation Analysis of SPAST, ATL1, and REEP1 in Korean Patients with Hereditary Spastic Paraplegia
  per: Kim, Tae-Hyoung, et al.
  Publicat: (2014)
• REEPing the benefits of an animal model of hereditary spastic paraplegia
  per: Deutch, Ariel Y., et al.
  Publicat: (2013)
• Subclinical cognitive impairment in autosomal dominant "pure" hereditary spastic paraplegia
  per: REID, E, et al.
  Publicat: (1999)