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Screening of Connexin 26 in Nonsyndromic Hearing Loss
Introduction The first locus for nonsyndromic autosomal recessive hearing loss is on chromosome 13q11–22. The 35delG mutation is present in 80% of cases in which GJB2 is involved, which makes the study of this mutation very important. The viability and benefits of screening for mutations in the conn...
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| Publicado en: | Int Arch Otorhinolaryngol |
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| Autores principales: | , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Thieme Publicações Ltda
2014
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4392499/ https://ncbi.nlm.nih.gov/pubmed/25992148 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0034-1373783 |
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