Hearing Loss
| dc.contributor.author | Coşar, Özlem Yüksel | |
| dc.contributor.author | Muluk, Nuray Bayar | |
| dc.contributor.author | Spremo, Slobodan | |
| dc.date.accessioned | 2025-01-21T16:27:41Z | |
| dc.date.available | 2025-01-21T16:27:41Z | |
| dc.date.issued | 2021 | |
| dc.department | Kırıkkale Üniversitesi | |
| dc.description.abstract | According to the majority of authorities on the subject, a genetic aetiology is implicated in 50% or more of cases of auditory loss [1–5]. Hearing loss may occur as part of a syndrome or in isolation. Just as in every genetic disorder, the inheritance pattern may be autosomal dominant (AD) or recessive (AR), X-linked, mitochondrial or a spontaneous mutation [6]. © The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Switzerland AG 2022. | |
| dc.identifier.doi | 10.1007/978-3-030-80691-0_15 | |
| dc.identifier.endpage | 190 | |
| dc.identifier.isbn | 978-303080691-0 | |
| dc.identifier.isbn | 978-303080690-3 | |
| dc.identifier.scopus | 2-s2.0-85156187429 | |
| dc.identifier.scopusquality | N/A | |
| dc.identifier.startpage | 179 | |
| dc.identifier.uri | https://doi.org/10.1007/978-3-030-80691-0_15 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12587/23398 | |
| dc.indekslendigikaynak | Scopus | |
| dc.language.iso | en | |
| dc.publisher | Springer International Publishing | |
| dc.relation.ispartof | Pediatric ENT Infections | |
| dc.relation.publicationcategory | Kitap Bölümü - Uluslararası | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.snmz | KA_20241229 | |
| dc.title | Hearing Loss | |
| dc.type | Book Chapter |
