The p.V37I Exclusive Genotype Of GJB2: A Genetic Risk-Indicator of Postnatal Permanent Childhood Hearing Impairment

Postnatal permanent childhood hearing impairment (PCHI) is frequent (0.25%–0.99%) and difficult to detect in the early stage, which may impede the speech, language and cognitive development of affected children. Genetic tests of common variants associated with postnatal PCHI in newborns may provide...

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Detalhes bibliográficos
Main Authors: Li, Lei, Lu, Jingrong, Tao, Zheng, Huang, Qi, Chai, Yongchuan, Li, Xiaohua, Huang, Zhiwu, Li, Yun, Xiang, Mingliang, Yang, Jun, Yao, Guoyin, Wang, Yu, Yang, Tao, Wu, Hao
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2012
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3344898/
https://ncbi.nlm.nih.gov/pubmed/22574200
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0036621
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