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GJB3/GJB6 screening in GJB2 carriers with idiopathic hearing loss: Is it necessary?
BACKGROUND: Genetic analysis detected excessive mono‐allelic recessive GJB2 mutations in individuals with idiopathic deafness; the remaining alleles in trans/cis are underdetermined. The aim of this study was to assess the contributions of variants in GJB3 or GJB6 to non‐syndromic sensorineural hear...
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| Publicat a: | J Clin Lab Anal |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley and Sons Inc.
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6817113/ https://ncbi.nlm.nih.gov/pubmed/29926981 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.22592 |
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