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

por Ghaedi, Hamid, Ramsheh, Samira Molaei, Omidvar, Maryam Erfanian, Labbaf, Afsaneh, Alehabib, Elham, Akbari, Sanaz, Pourfatemi, Fatemeh, Darvish, Hossein
Publicado 2019