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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Foilsithe in:Genes Dis
Main Authors: Ghaedi, Hamid, Ramsheh, Samira Molaei, Omidvar, Maryam Erfanian, Labbaf, Afsaneh, Alehabib, Elham, Akbari, Sanaz, Pourfatemi, Fatemeh, Darvish, Hossein
Formáid: Artigo
Teanga:Inglês
Foilsithe: Chongqing Medical University 2019
Ábhair:
Short Communication
Rochtain Ar Líne: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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