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The Relationship between the p.V37I Mutation in GJB2 and Hearing Phenotypes in Chinese Individuals
The most common cause of nonsyndromic autosomal recessive hearing loss is mutations in GJB2. The mutation spectrum and prevalence of mutations vary significantly among ethnic groups, and the relationship between p.V37I mutation in GJB2 and the hearing phenotype is controversial. Among the 3,864 pati...
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| Veröffentlicht in: | PLoS One |
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| Hauptverfasser: | , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Public Library of Science
2015
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4463851/ https://ncbi.nlm.nih.gov/pubmed/26061099 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0129662 |
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