Cargando…
High-throughput detection of mutations responsible for childhood hearing loss using resequencing microarrays
BACKGROUND: Despite current knowledge of mutations in 45 genes that can cause nonsyndromic sensorineural hearing loss (SNHL), no unified clinical test has been developed that can comprehensively detect mutations in multiple genes. We therefore designed Affymetrix resequencing microarrays capable of...
Autores principales: | , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2841091/ https://www.ncbi.nlm.nih.gov/pubmed/20146813 http://dx.doi.org/10.1186/1472-6750-10-10 |