Common molecular etiology of nonsyndromic hearing loss in 484 patients of 3 ethnicities in northwest China
Author:
Publisher
Informa UK Limited
Subject
Otorhinolaryngology,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.3109/00016489.2015.1006334
Reference20 articles.
1. Newborn and Infant Hearing Loss: Detection and Intervention
2. Newborn Hearing Screening — A Silent Revolution
3. Hereditary deafness and phenotyping in humans
4. Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene
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2. Low frequency of SLC26A4 c.919-2A > G variant among patients with nonsyndromic hearing loss in Yunnan of Southwest China;BMC Medical Genomics;2024-02-20
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