A Novel Mouse Model of MYO7A USH1B Reveals Auditory and Visual System Haploinsufficiencies

Usher’s syndrome is the most common combined blindness–deafness disorder with USH1B, caused by mutations in MYO7A, resulting in the most severe phenotype. The existence of numerous, naturally occurring shaker1 mice harboring variable MYO7A mutations on different genetic backgrounds has complicated t...

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Bibliografische gegevens
Gepubliceerd in:Front Neurosci
Hoofdauteurs: Calabro, Kaitlyn R., Boye, Sanford L., Choudhury, Shreyasi, Fajardo, Diego, Peterson, James J., Li, Wei, Crosson, Sean M., Kim, Mi-Jung, Ding, Dalian, Salvi, Richard, Someya, Shinichi, Boye, Shannon E.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Frontiers Media S.A. 2019
Onderwerpen:
Neuroscience
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6883748/
https://ncbi.nlm.nih.gov/pubmed/31824252
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnins.2019.01255
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