Φορτώνει......
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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Neurobiol Aging |
|---|---|
| Κύριοι συγγραφείς: | , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2019
|
| Θέματα: | |
| Διαθέσιμο Online: | 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 |
| Ετικέτες: |
Προσθήκη ετικέτας
Δεν υπάρχουν, Καταχωρήστε ετικέτα πρώτοι!
|