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Clinical Application of a Custom AmpliSeq Library and Ion Torrent PGM Sequencing to Comprehensive Mutation Screening for Deafness Genes
Background: Congenital hearing loss is one of the most common sensory disorders, with 50–70% of cases attributable to genetic causes. Although recent advances in the identification of deafness genes have resulted in more accurate molecular diagnosis, leading to the better determination of suitable c...
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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.
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4394162/ https://ncbi.nlm.nih.gov/pubmed/25587757 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/gtmb.2014.0252 |
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