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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...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Genet Test Mol Biomarkers |
|---|---|
| Prif Awduron: | , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Mary Ann Liebert, Inc.
2015
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| Pynciau: | |
| Mynediad Ar-lein: | 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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