Detection of 11 germline inactivating TP53 mutations and absence of TP63 and HCHK2 mutations in 17 French families with Li-Fraumeni or Li-Fraumeni-like syndrome

Samankaltaisia teoksia

• Inherited TP53 Mutations and the Li–Fraumeni Syndrome
  Tekijä: Guha, Tanya, et al.
  Julkaistu: (2017)
• Guidelines for the Li–Fraumeni and heritable TP53-related cancer syndromes
  Tekijä: Frebourg, Thierry, et al.
  Julkaistu: (2020)
• An extended Li-Fraumeni kindred with gastric carcinoma and a codon 175 mutation in TP53.
  Tekijä: Varley, J M, et al.
  Julkaistu: (1995)
• Germline TP53 Mutation and Clinical Characteristics of Korean Patients With Li-Fraumeni Syndrome
  Tekijä: Park, Kyoung-Jin, et al.
  Julkaistu: (2016)
• A mutation in the POT1 gene is responsible for cardiac angiosarcoma in TP53-negative Li–Fraumeni-like families
  Tekijä: Calvete, Oriol, et al.
  Julkaistu: (2015)