GJB2,SLC26A4and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects
Author:
Publisher
Informa UK Limited
Subject
Otorhinolaryngology,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1080/00016480701767382
Reference37 articles.
1. Genetic epidemiological studies of early-onset deafness in the U.S. school-age population
2. Genetic Epidemiology of Hearing Impairment
3. Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling
4. Hereditary sensorineural hearing loss: advances in molecular genetics and mutation analysis
5. Etiology of syndromic and nonsyndromic sensorineural hearing loss
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