Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

Παρόμοια τεκμήρια

• Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia
  ανά: Gan-Or, Ziv, κ.ά.
  Έκδοση: (2016)
• Mutation in the epsilon subunit of the cytosolic chaperonin‐containing t‐complex peptide‐1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic paraplegia
  ανά: Bouhouche, A, κ.ά.
  Έκδοση: (2006)
• Clinical and genetic data of Huntington disease in Moroccan patients
  ανά: Bouhouche, Ahmed, κ.ά.
  Έκδοση: (2015)
• From Learning to Memory: What Flies Can Tell Us about Intellectual Disability Treatment
  ανά: Androschuk, Alaura, κ.ά.
  Έκδοση: (2015)
• Transcriptomic Analysis of Zebrafish TDP-43 Transgenic Lines
  ανά: Lissouba, Alexandra, κ.ά.
  Έκδοση: (2018)