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Next-Generation Sequencing in Genetic Hearing Loss
The advent of the $1000 genome has the potential to revolutionize the identification of genes and their mutations underlying genetic disorders. This is especially true for extremely heterogeneous Mendelian conditions such as deafness, where the mutation, and indeed the gene, may be private. The rece...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Mary Ann Liebert, Inc.
2013
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3732417/ https://ncbi.nlm.nih.gov/pubmed/23738631 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/gtmb.2012.0464 |
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