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Combined examination of sequence and copy number variations in human deafness genes improves diagnosis for cases of genetic deafness
BACKGROUND: Copy number variations (CNVs) are the major type of structural variation in the human genome, and are more common than DNA sequence variations in populations. CNVs are important factors for human genetic and phenotypic diversity. Many CNVs have been associated with either resistance to d...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4194081/ https://ncbi.nlm.nih.gov/pubmed/25342930 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1472-6815-14-9 |
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