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Development of the stria vascularis and potassium regulation in the human fetal cochlea: Insights into hereditary sensorineural hearing loss

Sensorineural hearing loss (SNHL) is one of the most common congenital disorders in humans, afflicting one in every thousand newborns. The majority is of heritable origin and can be divided in syndromic and nonsyndromic forms. Knowledge of the expression profile of affected genes in the human fetal...

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Detaylı Bibliyografya
Yayımlandı:Dev Neurobiol
Asıl Yazarlar: Locher, Heiko, de Groot, John C.M.J., van Iperen, Liesbeth, Huisman, Margriet A., Frijns, Johan H.M., Chuva de Sousa Lopes, Susana M.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: John Wiley and Sons Inc. 2015
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5024031/
https://ncbi.nlm.nih.gov/pubmed/25663387
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/dneu.22279
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