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...

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Detalles Bibliográficos
Autores principales: Alsaber, Rami, Tabone, Christopher J, Kandpal, Raj P
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Methodology Article
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

Internet

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

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