Intestinal and extraintestinal neoplasms in patients with NTHL1 tumor syndrome: a systematic review
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Genetics (clinical),Oncology,Genetics
Link
https://link.springer.com/content/pdf/10.1007/s10689-022-00291-3.pdf
Reference27 articles.
1. Weren RDA et al (2015) A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer. Nat Genet 47(6):668–671. https://doi.org/10.1038/ng.3287
2. Weren RDA, Ligtenberg MJ, Geurts van Kessel A, de Voer RM, Hoogerbrugge N, Kuiper RP (2018) NTHL1 and MUTYH polyposis syndromes: two sides of the same coin? J Pathol 244(2):135–142. https://doi.org/10.1002/path.5002
3. Kuiper RP, Nielsen M, de Voer RM, Hoogerbrugge N (1993) NTHL1 tumor syndrome. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A (eds) Seattle (WA)
4. Altaraihi M, Gerdes AM, Wadt K (2019) A new family with a homozygous nonsense variant in NTHL1 further delineated the clinical phenotype of NTHL1-associated polyposis. Hum Genome Var 6(1):1–3. https://doi.org/10.1038/s41439-019-0077-3
5. Belhadj S et al (2017) Delineating the phenotypic spectrum of the NTHL1-associated polyposis. Clin Gastroenterol Hepatol 15(3):461–462. https://doi.org/10.1016/J.CGH.2016.09.153
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