Second Case of Tumors Associated With Heterozygous NTHL1 Variant

Homozygous mutations to NTHL1 are known to increase cancer risk, particularly in the colon and breast. NTHL1 tumor syndrome (NTS) is an autosomal recessive genetic condition. Little is known about the cancer risk in patients who have heterozygous NTHL1 mutations. We previously published a case of be...

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Detalles Bibliográficos
Autores principales: Anderson, Danyon J, Reinicke, Trenton, Boyle, Andrew W, Porwal, Mokshal H, Friedman, Allan H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364427/
https://www.ncbi.nlm.nih.gov/pubmed/35967160
http://dx.doi.org/10.7759/cureus.26734

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364427/
https://www.ncbi.nlm.nih.gov/pubmed/35967160
http://dx.doi.org/10.7759/cureus.26734

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