Gamma knife radiotherapy in a neurofibromatosis type 1 Chinese pedigrees with NF1 gene frameshift mutation: A case report

RATIONALE: Neurofibromatosis type 1 (NF1) is a common autosomal dominant genetic disorder. NF1 is a multisystemic disease and its pathogenesis involves mutations in the NF1 gene on chromosome 17q11.2 causing RAS overactivation to stimulate abnormal cell proliferation. In this article, a Chinese fami...

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Detalles Bibliográficos
Autores principales: Dong, Meng-Jie, Yang, Zhong-Kun, Yang, Ji, Guo, Rui-Qin, Xiao, Yu-Yuan, Liu, Hai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9259110/
https://www.ncbi.nlm.nih.gov/pubmed/35801779
http://dx.doi.org/10.1097/MD.0000000000029280

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9259110/
https://www.ncbi.nlm.nih.gov/pubmed/35801779
http://dx.doi.org/10.1097/MD.0000000000029280

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