Audiologic Phenotype and Progression in GJB2 (Connexin 26) Hearing Loss

OBJECTIVES: To document the audiologic phenotype of children with biallelic GJB2 (connexin 26) mutations, and to correlate it with the genotype. DESIGN: Prospective, observational study. SETTING: Tertiary care children’s hospital. PATIENTS: Infants and children with sensorineural hearing loss (SNHL)...

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Bibliografiske detaljer
Udgivet i:Arch Otolaryngol Head Neck Surg
Main Authors: Kenna, Margaret A., Feldman, Henry A., Neault, Marilyn W., Frangulov, Anna, Wu, Bai-Lin, Fligor, Brian, Rehm, Heidi L.
Format: Artigo
Sprog:Inglês
Udgivet: 2010
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Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4528189/
https://ncbi.nlm.nih.gov/pubmed/20083784
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/archoto.2009.202
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