Whole-exome sequencing identified a novel mutation of MLH1 in an extended family with lynch syndrome

Hereditary nonpolyposis colorectal cancer or Lynch syndrome is autosomal dominant cancer predisposition syndrome characterized by early onset of colorectal cancer and neoplasia in other organs. This condition typically caused by germline mutations in the mismatch repair genes MLH1, MSH2, MSH6, and P...

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Detalhes bibliográficos
Publicado no:Genes Dis
Main Authors: Ghaedi, Hamid, Ramsheh, Samira Molaei, Omidvar, Maryam Erfanian, Labbaf, Afsaneh, Alehabib, Elham, Akbari, Sanaz, Pourfatemi, Fatemeh, Darvish, Hossein
Formato: Artigo
Idioma:Inglês
Publicado em: Chongqing Medical University 2019
Assuntos:
Short Communication
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7729095/
https://ncbi.nlm.nih.gov/pubmed/33335961
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gendis.2019.07.011
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