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...

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Detalles Bibliográficos
Autores principales: Xu, Min, Xiong, Hui, Han, Yanfang, Li, Chijun, Mai, Shaozhen, Huang, Zhongzhou, Ai, Xuechen, Guo, Zhixuan, Zeng, Fanqin, Guo, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6066643/
https://www.ncbi.nlm.nih.gov/pubmed/30087692
http://dx.doi.org/10.3389/fgene.2018.00270

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