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Allele specific oligonucleotide analysis of the common deafness mutation 35delG in the connexin 26 (GJB2) gene

Despite the large number of genes that are expected to be involved in non-syndromal, recessive deafness, only a few have been cloned. One of these genes is GJB2, which encodes connexin 26.( )A frameshift mutation in this gene has been reported to be common in several populations and a carrier freque...

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Detalles Bibliográficos
Main Authors: Rabionet, R., Estivill, X.
Formato: Artigo
Idioma:Inglês
Publicado: BMJ Group 1999
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC1734314/
https://ncbi.nlm.nih.gov/pubmed/10204859
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