Publisher Correction: Molecular mechanisms of Charcot-Marie-Tooth neuropathy linked to mutations in human myelin protein P2

Những quyển sách tương tự

• Molecular mechanisms of Charcot-Marie-Tooth neuropathy linked to mutations in human myelin protein P2
  Bằng: Ruskamo, Salla, et al.
  Được phát hành: (2017)
• Structure and dynamics of a human myelin protein P2 portal region mutant indicate opening of the β barrel in fatty acid binding proteins
  Bằng: Laulumaa, Saara, et al.
  Được phát hành: (2018)
• Cryo-EM, X-ray diffraction, and atomistic simulations reveal determinants for the formation of a supramolecular myelin-like proteolipid lattice
  Bằng: Ruskamo, Salla, et al.
  Được phát hành: (2020)
• Neuropathy-related mutations alter the membrane binding properties of the human myelin protein P0 cytoplasmic tail
  Bằng: Raasakka, Arne, et al.
  Được phát hành: (2019)
• How Does Protein Zero Assemble Compact Myelin?
  Bằng: Raasakka, Arne, et al.
  Được phát hành: (2020)