The Founder Mutation MSH2*1906G→C Is an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Ashkenazi Jewish Population

Hereditary nonpolyposis colorectal cancer (HNPCC) is caused by mutations in the mismatch-repair genes. We report here the identification and characterization of a founder mutation in MSH2 in the Ashkenazi Jewish population. We identified a nucleotide substitution, MSH2*1906G→C, which results in a su...

ver descrição completa

Detalhes bibliográficos

Publicado no:	Am J Hum Genet
Principais autores:	Foulkes, W. D., Thiffault, I., Gruber, S. B., Horwitz, M., Hamel, N., Lee, C., Shia, J., Markowitz, A., Figer, A., Friedman, E., Farber, D., Greenwood, C. M. T., Bonner, J. D., Nafa, K., Walsh, T., Marcus, V., Tomsho, L., Gebert, J., Macrae, F. A., Gaff, C. L., Paillerets, B. Bressac-de, Gregersen, P. K., Weitzel, J. N., Gordon, P. H., MacNamara, E., King, M.-C., Hampel, H., de la Chapelle, A., Boyd, J., Offit, K., Rennert, G., Chong, G., Ellis, N. A.
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Elsevier 2002
Assuntos:	Articles
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC420003/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12454801/ https://ncbi.nlm.nih.govhttps://doi.org/10.1086/345075
Tags:	Adicionar Tag Sem tags, seja o primeiro a adicionar uma tag!