Complete STK11 Deletion and Atypical Symptoms in Peutz-Jeghers Syndrome

Antzeko izenburuak

• Exonic STK11 deletions are not a rare cause of Peutz‐Jeghers syndrome
  nork: Hearle, N C M, et al.
  Argitaratua: (2006)
• Peutz-Jeghers syndrome with germline mutation of STK11
  nork: Chae, Hyun-Dong, et al.
  Argitaratua: (2014)
• STK11 genotyping and cancer risk in Peutz-Jeghers syndrome
  nork: Schumacher, V, et al.
  Argitaratua: (2005)
• STK11 status and intussusception risk in Peutz‐Jeghers syndrome
  nork: Hearle, N, et al.
  Argitaratua: (2006)
• Mutations in STK11 gene in Czech Peutz-Jeghers patients
  nork: Vasovčák, Peter, et al.
  Argitaratua: (2009)