Associated Papers
Clinical perspectives on the value of testing for STK11 and KEAP1 mutations in advanced NSCLC.
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Frontiers in Oncology, 2024
39703851 (PubMed )
Supplement: DataSheet2.xlsx › Supplemental_data
STK11 Causative Variants and Copy Number Variations Identified in Thai Patients With Peutz-Jeghers Syndrome.
Chiraphapphaiboon W et al.
Cureus, 2023
STK11 domain XI mutations: candidate genetic drivers leading to the development of dysplastic polyps in Peutz-Jeghers syndrome.
Wang Z et al.
Human Mutation, 2014
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