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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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| Publicat a: | Otol Neurotol |
|---|---|
| Autors principals: | , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2020
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| Matèries: | |
| Accés en línia: | 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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