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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344898/
https://www.ncbi.nlm.nih.gov/pubmed/22574200
http://dx.doi.org/10.1371/journal.pone.0036621

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344898/
https://www.ncbi.nlm.nih.gov/pubmed/22574200
http://dx.doi.org/10.1371/journal.pone.0036621

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