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Genomics, Epigenetics, and Hearing Loss in Neurofibromatosis Type 2

OBJECTIVES: In this review, we discuss current knowledge about the genetics and epigenetics of vestibular schwannoma (VS) in relation to hearing loss. A multi-step and sequential genetic algorithm suitable for the identification of Neurofibromatosis Type 2 (NF2) constitutional and somatic mutations...

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Detalhes bibliográficos
Publicado no:Otol Neurotol
Main Authors: Dinh, Christine T., Nisenbaum, Eric, Chyou, Darius, Misztal, Carly, Yan, Denise, Mittal, Rahul, Young, Juan, Tekin, Mustafa, Telischi, Fred, Fernandez-Valle, Cristina, Liu, Xue-Zhong
Formato: Artigo
Idioma:Inglês
Publicado em: 2020
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7547625/
https://ncbi.nlm.nih.gov/pubmed/32150022
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MAO.0000000000002613
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