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...

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Hoofdauteurs: Kothiyal, Prachi, Cox, Stephanie, Ebert, Jonathan, Husami, Ammar, Kenna, Margaret A, Greinwald, John H, Aronow, Bruce J, Rehm, Heidi L
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BioMed Central 2010
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Research article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2841091/
https://ncbi.nlm.nih.gov/pubmed/20146813
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1472-6750-10-10
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