No immediate practice change; these newly identified LOXHD1 variants are a preliminary genetic finding that may improve the diagnostic yield of genetic hearing loss panels in future, but clinical utility depends on further validation studies.

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PubMed·Journal article·Research (general)·7w ago

Identification of Novel LOXHD1 Variants in Chinese Patients with Non-Syndromic Hearing Loss

No immediate change to clinical practice, but these novel LOXHD1 variants expand the genetic panel targets relevant for late-onset non-syndromic hearing loss in East Asian populations.

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