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See Latest ArticlesIdentification of Novel Variants in the Cx29 Gene of Nonsyndromic Hearing Loss Patients Using Buccal Cells and Restriction Fragment Length Polymorphism Method
Audiology & Neuro-Otology, 08/04/09
Wang WH et al. – The authors suggest that the c.[43CG(+)230GC] compound heterozygous variant of Cx29 may be a risk factor for the development of hearing loss in Taiwanese and that the restriction fragment length polymorphism method developed will be clinically useful in identifying variants of the Cx29 gene in patients with hearing loss.
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