Prevalence of GJB2 mutations and the del(GJB6-D13S1830) in Argentinean non-syndromic deaf patients
Author:
Publisher
Elsevier BV
Subject
Sensory Systems
Reference36 articles.
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2. Loss-of-function and residual channel activity of connexin 26 mutations associated with non-syndromic deafness;Bruzzone;FEBS Lett.,2003
3. Deafness genes and their diagnostic applications;Cryns;Audiol. Neurootol.,2004
4. A deletion involving the connexin 30 gene in nonsyndromic hearing impairment;del Castillo;New Eng. J. Med.,2002
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