Somatic STK11 mosaicism in a Turkish patient with Peutz-Jeghers syndrome
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s10689-024-00405-z.pdf
Reference13 articles.
1. Wagner A, Aretz S, Auranen A, Bruno MJ, Cavestro GM, Crosbie EJ, Goverde A, Jelsig AM, Latchford A, Leerdam MEV, Lepisto A, Puzzono M, Winship I, Zuber V, Möslein G (2021) The management of Peutz-Jeghers Syndrome: European Hereditary Tumour Group (EHTG) Guideline. J Clin Med 10(3):473. https://doi.org/10.3390/jcm10030473
2. Jelsig AM, Karstensen JG, Overeem Hansen TV (2024) Progress report: Peutz-Jeghers syndrome. Fam Cancer 16. https://doi.org/10.1007/s10689-024-00362-7Epub ahead of print
3. Jelsig AM, Wullum L, Kuhlmann TP, Ousager LB, Burisch J, Karstensen JG (2023) Risk of Cancer and Mortality in Peutz-Jeghers Syndrome and Juvenile Polyposis Syndrome-A Nationwide Cohort Study with matched controls. Gastroenterology 165(6):1565–1567e2. https://doi.org/10.1053/j.gastro.2023.08.040
4. Tacheci I, Kopacova M, Bures J (2021) Peutz-Jeghers syndrome. Curr Opin Gastroenterol 37:245–254. https://doi.org/10.1097/MOG.0000000000000718
5. McKay V, Cairns D, Gokhale D et al (2016) First report of somatic mosaicism for mutations in STK11 in four patients with Peutz-Jeghers syndrome. Fam Cancer 15:57–61. https://doi.org/10.1007/s10689-015-9839-3
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