Cargando…
Inner Ear Morphology Is Perturbed in Two Novel Mouse Models of Recessive Deafness
Human MYO7A mutations can cause a variety of conditions involving the inner ear. These include dominant and recessive non-syndromic hearing loss and syndromic conditions such as Usher syndrome. Mouse models of deafness allow us to investigate functional pathways involved in normal and abnormal heari...
Autores principales: | Miller, Kerry A., Williams, Louise H., Rose, Elizabeth, Kuiper, Michael, Dahl, Hans-Henrik M., Manji, Shehnaaz S. M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520982/ https://www.ncbi.nlm.nih.gov/pubmed/23251483 http://dx.doi.org/10.1371/journal.pone.0051284 |
Ejemplares similares
-
Eeyore: A Novel Mouse Model of Hereditary Deafness
por: Miller, Kerry A., et al.
Publicado: (2013) -
A Mutation in Synaptojanin 2 Causes Progressive Hearing Loss in the ENU-Mutagenised Mouse Strain Mozart
por: Manji, Shehnaaz S. M., et al.
Publicado: (2011) -
Cochlear morphology in the developing inner ear of the porcine model of spontaneous deafness
por: Chen, Wei, et al.
Publicado: (2018) -
Deafness-in-a-dish: modeling hereditary deafness with inner ear organoids
por: Romano, Daniel R., et al.
Publicado: (2021) -
Imaging assessment of profound sensorineural deafness with inner ear anatomical abnormalities
por: Wu, Wei-Jing, et al.
Publicado: (2015)