Spinal Muscular Atrophy with Pontocerebellar Hypoplasia Is Caused by a Mutation in the VRK1 Gene

Những quyển sách tương tự

• The Spinal Muscular Atrophy with Pontocerebellar Hypoplasia Gene VRK1 Regulates Neuronal Migration through an Amyloid-β Precursor Protein-Dependent Mechanism
  Bằng: Vinograd-Byk, Hadar, et al.
  Được phát hành: (2015)
• Vrk1 partial Knockdown in Mice Results in Reduced Brain Weight and Mild Motor Dysfunction, and Indicates Neuronal VRK1 Target Pathways
  Bằng: Vinograd-Byk, Hadar, et al.
  Được phát hành: (2018)
• De Novo Variant in KIF26B isAssociated with Pontocerebellar Hypoplasia with Infantile Spinal Muscular Atrophy
  Bằng: Wojcik, Monica H., et al.
  Được phát hành: (2018)
• Novel motor phenotypes in patients with VRK1 mutations without pontocerebellar hypoplasia
  Bằng: Stoll, Marion, et al.
  Được phát hành: (2016)
• Adult-Onset Spinal Muscular Atrophy due to Mutations in the VRK1 Gene
  Bằng: Sung, Angela, et al.
  Được phát hành: (2021)