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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Enregistré dans:
Détails bibliographiques
Publié dans:OMICS
Auteurs principaux: Bosch, Jason, Noubiap, Jean Jacques N., Dandara, Collet, Makubalo, Nomlindo, Wright, Galen, Entfellner, Jean-Baka Domelevo, Tiffin, Nicki, Wonkam, Ambroise
Format: Artigo
Langue:Inglês
Publié: Mary Ann Liebert, Inc. 2014
Sujets:
Original Articles
Accès en ligne: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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