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Genomics, Epigenetics, and Hearing Loss in Neurofibromatosis Type 2

5 Mar 2020

Abstract excerpt

OBJECTIVES: In this review, we discuss current knowledge about the genetics and epigenetics of vestibular schwannoma (VS) in relation to hearing loss. A multistep and sequential genetic algorithm suitable for the identification of Neurofibromatosis Type 2 (NF2) constitutional and somatic mutations is discussed. DATA SOURCES, STUDY SELECTION: A review was performed of the English literature from 1990 to 2019 using...

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PMID: 32150022
DOI: 10.1097/mao.0000000000002613

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