High frequency of connexin26 (GJB2) mutations associated with nonsyndromic hearing loss in the population of Kerala, India
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology, and Child Health
Reference21 articles.
1. Genetic epidemiology of hearing impairment;Morton;Ann. N. Y. Acad. Sci.,1991
2. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness;Kelsell;Nature,1997
3. Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene;Denoyelle;Hum. Mol. Genet.,1997
4. Connexin-26 mutations in sporadic and inherited sensorineural deafness;Estivill;Lancet,1998
5. High frequency of the deafness-associated 167delT mutation in the connexin 26 (GJB2) gene in Israeli Ashkenazim;Sobe;Am. J. Med. Genet.,1999
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