GJB2 and GJB6 Mutations in Non-Syndromic Childhood Hearing Impairment in Ghana

Our study aimed to investigate GJB2 (connexin 26) and GJB6 (connexin 30) mutations associated with non-syndromic childhood hearing impairment (HI) as well as the environmental causes of HI in Ghana. Medical reports of 1,104 students attending schools for the deaf were analyzed. Families segregating...

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Detalles Bibliográficos
Publicado en:Front Genet
Main Authors: Adadey, Samuel M., Manyisa, Noluthando, Mnika, Khuthala, de Kock, Carmen, Nembaware, Victoria, Quaye, Osbourne, Amedofu, Geoffrey K., Awandare, Gordon A., Wonkam, Ambroise
Formato: Artigo
Idioma:Inglês
Publicado: Frontiers Media S.A. 2019
Assuntos:
Genetics
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6759689/
https://ncbi.nlm.nih.gov/pubmed/31620164
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2019.00841
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