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Predicting candidate genes for human deafness disorders: a bioinformatics approach
BACKGROUND: There are more than 50 genes for autosomal dominant and autosomal recessive nonsyndromic hereditary deafness that are yet to be cloned. The human genome sequence and expression profiles of transcripts in the inner ear have aided positional cloning approaches. The knowledge of protein int...
| Autores principales: | , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2006
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1564145/ https://www.ncbi.nlm.nih.gov/pubmed/16854223 http://dx.doi.org/10.1186/1471-2164-7-180 |