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NF1 Mutations Analysis Using Whole Exome Sequencing Technique in 11 Unrelated Iranian Families with Neurofibromatosis Type 1
NF1 Mutations Analysis Using Whole Exome Sequencing Technique in 11 Unrelated Iranian Families with Neurofibromatosis Type 1

Samira Foji; Saeed Dorgaleleh; Morteza Oladnabi; Leila Jouybari

Volume 8, Issue 5 , May 2020, , Pages 11311-11319

https://doi.org/10.22038/ijp.2020.46890.3804

Abstract
  Background Neurofibromatosis is an autosomal dominant disease. It affects one in 2,700 to 3,300 people. The main gene mutated in the disease is a tumor suppressor protein called neurofibromin. ...  Read More