Monoallelic NTHL1 Loss-of-Function Variants and Risk of Polyposis and Colorectal Cancer

Ítems similars

• Colorectal Cancer Risk in Monoallelic Carriers of MYH Variants
  per: Webb, Emily L., et al.
  Publicat: (2006)
• A new family with a homozygous nonsense variant in NTHL1 further delineated the clinical phenotype of NTHL1-associated polyposis
  per: Altaraihi, Mays, et al.
  Publicat: (2019)
• Candidate Gene Discovery in Hereditary Colorectal Cancer and Polyposis Syndromes–Considerations for Future Studies
  per: te Paske, Iris B. A. W., et al.
  Publicat: (2020)
• Low frequency of POLD1 and POLE exonuclease domain variants in patients with multiple colorectal polyps
  per: Elsayed, Fadwa A., et al.
  Publicat: (2019)
• Prevalence and Characterization of Biallelic and Monoallelic NTHL1 and MSH3 Variant Carriers From a Pan-Cancer Patient Population
  per: Salo-Mullen, Erin E., et al.
  Publicat: (2021)