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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Dettagli Bibliografici
Pubblicato in:Front Neurosci
Autori principali: 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.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Frontiers Media S.A. 2019
Soggetti:
Neuroscience
Accesso online: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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