The contribution of GJB2 mutations to slight or mild hearing loss in Australian elementary school children

Background: There is a lack of information on prevalence, cause and consequences of slight/mild bilateral sensorineural hearing loss (SNHL) in children. We report the first systematic genetic analysis of the GJB2 gene in a population‐derived sample of children with slight/mild bilateral SNHL. Method...

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Detalhes bibliográficos
Main Authors: Dahl, H‐H M, Tobin, S E, Poulakis, Z, Rickards, F W, Xu, X, Gillam, L, Williams, J, Saunders, K, Cone‐Wesson, B, Wake, M
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2006
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2563186/
https://ncbi.nlm.nih.gov/pubmed/16840571
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2006.042051
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