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Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss
Aim: To investigate the causative genetic mutations in 12 Pakistani families with nonsyndromic or syndromic hearing loss. Methods: Mutations in the most common causative gene for hearing loss, GJB2, were evaluated by Sanger sequencing. Targeted next-generation sequencing or whole-exome sequencing wa...
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| Publicado no: | Genet Test Mol Biomarkers |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Mary Ann Liebert, Inc.
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5444417/ https://ncbi.nlm.nih.gov/pubmed/28281779 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/gtmb.2016.0328 |
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