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Cochlear Implantation Outcome in Children with DFNB1 locus Pathogenic Variants
Almost 60% of children with profound prelingual hearing loss (HL) have a genetic determinant of deafness, most frequently two DFNB1 locus (GJB2/GJB6 genes) recessive pathogenic variants. Only few studies combine HL etiology with cochlear implantation (CI) outcome. Patients with profound prelingual H...
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| Publicat a: | J Clin Med |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
MDPI
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7019930/ https://ncbi.nlm.nih.gov/pubmed/31952308 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm9010228 |
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