Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11

Παρόμοια τεκμήρια

• Mutations in phospholipase DDHD2 cause autosomal recessive hereditary spastic paraplegia (SPG54)
  ανά: Gonzalez, Michael, κ.ά.
  Έκδοση: (2013)
• High frequency of SPG4 in Taiwanese families with autosomal dominant hereditary spastic paraplegia
  ανά: Lan, Min-Yu, κ.ά.
  Έκδοση: (2014)
• MR Imaging Findings in Autosomal Recessive Hereditary Spastic Paraplegia
  ανά: Hourani, R., κ.ά.
  Έκδοση: (2009)
• Case Series of Autosomal Recessive Hereditary Spastic Paraplegia in Adults
  ανά: Chakor, Rahul T., κ.ά.
  Έκδοση: (2021)
• Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia
  ανά: Gan-Or, Ziv, κ.ά.
  Έκδοση: (2016)