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Gene replacement therapy in a schwannoma mouse model of neurofibromatosis type 2

Loss of function of the neurofibromatosis type 2 (NF2) tumor suppressor gene leads to the formation of schwannomas, meningiomas, and ependymomas, comprising ∼50% of all sporadic cases of primary nervous system tumors. NF2 syndrome is an autosomal dominant condition, with bi-allelic inactivation of g...

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Bibliographic Details
Main Authors: Prabhakar, Shilpa, Beauchamp, Roberta L., Cheah, Pike See, Yoshinaga, Akiko, Haidar, Edwina Abou, Lule, Sevda, Mani, Gayathri, Maalouf, Katia, Stemmer-Rachamimov, Anat, Jung, David H., Welling, D. Bradley, Giovannini, Marco, Plotkin, Scott R., Maguire, Casey A., Ramesh, Vijaya, Breakefield, Xandra O.
Format: Article
Published: Cell Press 2022
Online Access:http://psasir.upm.edu.my/id/eprint/101608/
https://www.sciencedirect.com/science/article/pii/S2329050122000912?via%3Dihub
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http://psasir.upm.edu.my/id/eprint/101608/
https://www.sciencedirect.com/science/article/pii/S2329050122000912?via%3Dihub

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