A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1–12q14

Antzeko izenburuak

• Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11
  nork: Chen, Xueping, et al.
  Argitaratua: (2020)
• Mutations in phospholipase DDHD2 cause autosomal recessive hereditary spastic paraplegia (SPG54)
  nork: Gonzalez, Michael, et al.
  Argitaratua: (2013)
• MR Imaging Findings in Autosomal Recessive Hereditary Spastic Paraplegia
  nork: Hourani, R., et al.
  Argitaratua: (2009)
• Case Series of Autosomal Recessive Hereditary Spastic Paraplegia in Adults
  nork: Chakor, Rahul T., et al.
  Argitaratua: (2021)
• Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia
  nork: Gan-Or, Ziv, et al.
  Argitaratua: (2016)