Pure hereditary spastic paraplegia due to a de-novo mutation in the NIPA1 gene

समान संसाधन

• De novo REEP2 missense mutation in pure hereditary spastic paraplegia
  द्वारा: Roda, Ricardo H., और अन्य
  प्रकाशित: (2017)
• Pure hereditary spastic paraplegia.
  द्वारा: Reid, E
  प्रकाशित: (1997)
• NIPA1 Gene Mutations Cause Autosomal Dominant Hereditary Spastic Paraplegia (SPG6)
  द्वारा: Rainier, Shirley, और अन्य
  प्रकाशित: (2003)
• Pure or Complex Hereditary Spastic Paraplegia Type 4?
  द्वारा: Finsterer, Josef
  प्रकाशित: (2019)
• TDP-43 Pathology in a Case of Hereditary Spastic Paraplegia with a NIPA1/SPG6 Mutation
  द्वारा: Martinez-Lage, Maria, और अन्य
  प्रकाशित: (2012)