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Clinical comparison of hearing impaired patients with DFNB1 against heterozygote carriers of connexin 26 mutations

OBJECTIVE: The aim of the study is to assess clinical characteristics of individuals with non-syndromic sensorineural hearing loss (NSSNHL) with genetic mutations in GJB2 and/or GJB6. We describe and compare one group with biallelic mutations against a group of heterozygote mutation carriers. SUBJEC...

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Detalhes bibliográficos
Main Authors: Lipan, Michael, Ouyang, Xiaomei, Yan, Denise, Angeli, Simon, Du, Li Lin, Liu, Xue-Zhong
Formato: Artigo
Idioma:Inglês
Publicado em: 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3065787/
https://ncbi.nlm.nih.gov/pubmed/21287563
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/lary.21422
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