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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Vydáno v:Dev Neurobiol
Hlavní autoři: Locher, Heiko, de Groot, John C.M.J., van Iperen, Liesbeth, Huisman, Margriet A., Frijns, Johan H.M., Chuva de Sousa Lopes, Susana M.
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2015
Témata:
Research Articles
On-line přístup: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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