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Mice heterozygous for the Cdh23/Ahl1 Mutation Show Age-Related Deficits in Auditory Temporal Processing

A mutation in the Cdh23 gene is implicated in both syndromic and non-syndromic hearing loss in humans and age-related hearing loss in C57BL/6 mice. It is generally assumed that human patients (as well as mouse models) only have a hearing loss phenotype if the mutation is homozygous. However, a major...

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Bibliografske podrobnosti
izdano v:Neurobiol Aging
Main Authors: Burghard, Alice L., Morel, Nazli P., Oliver, Douglas L.
Format: Artigo
Jezik:Inglês
Izdano: 2019
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6732241/
https://ncbi.nlm.nih.gov/pubmed/31247458
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neurobiolaging.2019.02.029
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