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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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| Publicado no: | Arch Otolaryngol Head Neck Surg |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | 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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