A murine model of neurofibromatosis type 2 that accurately phenocopies human schwannoma formation

Neurofibromatosis type 2 (NF2) is an autosomal dominant genetic disorder resulting from germline mutations in the NF2 gene. Bilateral vestibular schwannomas, tumors on cranial nerve VIII, are pathognomonic for NF2 disease. Furthermore, schwannomas also commonly develop in other cranial nerves, dorsa...

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Publicado no:Hum Mol Genet
Main Authors: Gehlhausen, Jeffrey R., Park, Su-Jung, Hickox, Ann E., Shew, Matthew, Staser, Karl, Rhodes, Steven D., Menon, Keshav, Lajiness, Jacquelyn D., Mwanthi, Muithi, Yang, Xianlin, Yuan, Jin, Territo, Paul, Hutchins, Gary, Nalepa, Grzegorz, Yang, Feng-Chun, Conway, Simon J., Heinz, Michael G., Stemmer-Rachamimov, Anat, Yates, Charles W., Wade Clapp, D.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2015
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4262489/
https://ncbi.nlm.nih.gov/pubmed/25113746
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu414
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