Characterization of New Founder Alu-Mediated Rearrangements in MSH2 Gene Associated with a Lynch Syndrome Phenotype

Autor: Perez-Cabornero, L, Flores, EB, Sanz, MI, Sampedro, EV, Becares, AA, Aras, EL, Gonzalez, JC, Riu, MP, Asensio, TRYC, Munar, GC, Pino, CM, Dominguez, MD

Publikováno v: Cancer Prevention Research
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
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It has been reported that large genomic deletions in the MLH1 and MSH2 genes are a frequent cause of Lynch syndrome in certain populations. Here, a cohort has been screened and two new founder rearrangements have been found in the MSH2 gene. These mu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::9a429d3319b4ba697d5dacc761f2ba88
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=11698