Loss of p53 Sensitizes Mice with a Mutation in Ccm1 (KRIT1) to Development of Cerebral Vascular Malformations

Lignende værker

• Novel KRIT1/CCM1 and MGC4607/CCM2 Gene Variants in Chinese Families With Cerebral Cavernous Malformations
  af: Wang, Kang, et al.
  Udgivet: (2018)
• Loss of cerebral cavernous malformation 3 (Ccm3) in neuroglia leads to CCM and vascular pathology
  af: Louvi, Angeliki, et al.
  Udgivet: (2011)
• Novel KRIT1/CCM1 mutation in a patient with retinal cavernous hemangioma and cerebral cavernous malformation
  af: Reddy, Shantan, et al.
  Udgivet: (2010)
• Two Novel KRIT1 and CCM2 Mutations in Patients Affected by Cerebral Cavernous Malformations: New Information on CCM2 Penetrance
  af: Concetta Scimone, et al.
  Udgivet: (2018-11-01)
• Two Novel KRIT1 and CCM2 Mutations in Patients Affected by Cerebral Cavernous Malformations: New Information on CCM2 Penetrance
  af: Scimone, Concetta, et al.
  Udgivet: (2018)