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A novel stop codon mutation in STK11 gene is associated with Peutz-Jeghers Syndrome and elevated cancer risk: a case

Binazir Khanabadi1, Diba Najafgholizadeh Seyfi1, Leili Rejali1

  • 1Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Gastroenterology and Hepatology From Bed to Bench
|September 28, 2023
PubMed

Keywords:
Genetic analysisNovel mutationPeutz-Jeghers syndrome (PJS)STK11geneSequencing

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