81252 Gjb2 gene full sequence
Pathology & Lab
Also known as: GJB2 sequencing, Connexin 26 gene analysis
Complete sequence analysis of the GJB2 gene to identify mutations associated with non-syndromic hearing loss.
Clinical Context
Used to diagnose non-syndromic hearing loss caused by GJB2 mutations, the most common genetic cause of deafness.
RVU Breakdown
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Specialties
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