Sequencing of GJB2 in Cameroonians and Black South Africans and comparison to 1000 Genomes Project Data Support Need to Revise Strategy for Discovery of Nonsyndromic Deafness Genes in Africans

Mutations in the GJB2 gene, encoding connexin 26, could account for 50% of congenital, nonsyndromic, recessive deafness cases in some Caucasian/Asian populations. There is a scarcity of published data in sub-Saharan Africans. We Sanger sequenced the coding region of the GJB2 gene in 205 Cameroonian...

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Detalhes bibliográficos
Publicado no:OMICS
Main Authors: Bosch, Jason, Noubiap, Jean Jacques N., Dandara, Collet, Makubalo, Nomlindo, Wright, Galen, Entfellner, Jean-Baka Domelevo, Tiffin, Nicki, Wonkam, Ambroise
Formato: Artigo
Idioma:Inglês
Publicado em: Mary Ann Liebert, Inc. 2014
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5206689/
https://ncbi.nlm.nih.gov/pubmed/25162826
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/omi.2014.0063
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