Identification of Mutation Regions on NF1 Responsible for High- and Low-Risk Development of Optic Pathway Glioma in Neurofibromatosis Type I

Neurofibromatosis type I is a rare neurocutaneous syndrome resulting from loss-of-function mutations of NF1. The present study sought to determine a correlation between mutation regions on NF1 and the risk of developing optic pathway glioma (OPG) in patients with neurofibromatosis type I. A total of...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Front Genet
Main Authors: Xu, Min, Xiong, Hui, Han, Yanfang, Li, Chijun, Mai, Shaozhen, Huang, Zhongzhou, Ai, Xuechen, Guo, Zhixuan, Zeng, Fanqin, Guo, Qing
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2018
Assuntos:
Genetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6066643/
https://ncbi.nlm.nih.gov/pubmed/30087692
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2018.00270
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados