Deletions in CCM2 Are a Common Cause of Cerebral Cavernous Malformations

Những quyển sách tương tự

• Mutations in a Gene Encoding a Novel Protein Containing a Phosphotyrosine-Binding Domain Cause Type 2 Cerebral Cavernous Malformations
  Bằng: Liquori, Christina L., et al.
  Được phát hành: (2003)
• Lesions from patients with sporadic cerebral cavernous malformations harbor somatic mutations in the CCM genes: evidence for a common biochemical pathway for CCM pathogenesis
  Bằng: McDonald, David A., et al.
  Được phát hành: (2014)
• CCM3 and cerebral cavernous malformation disease
  Bằng: Wang, Kang, et al.
  Được phát hành: (2019)
• Recent insights into cerebral cavernous malformations: animal models of CCM and the human phenotype
  Bằng: Chan, Aubrey C., et al.
  Được phát hành: (2010)
• Biallelic somatic and germline mutations in cerebral cavernous malformations (CCMs): evidence for a two-hit mechanism of CCM pathogenesis
  Bằng: Akers, Amy L., et al.
  Được phát hành: (2009)