Identification of Novel LOXHD1 Variants in Chinese Patients with Non-Syndromic Hearing Loss
Objectives Although LOXHD1 mutations have been increasingly implicated in late-onset hereditary hearing loss, the genetic spectrum and underlying molecular mechanisms in the Chinese population remain inadequately characterized. This study aims to delineate the genetic landscape of LOXHD1 in Chinese...
Gorde:
| Egile Nagusiak: | , , , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Tsinghua University Press
2026-04-01
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| Saila: | Journal of Otology |
| Gaiak: | |
| Sarrera elektronikoa: | https://www.sciopen.com/article/10.26599/JOTO.2026.9540055 |
| Etiketak: |
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