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myosin 7aa(−/−) mutant zebrafish show mild photoreceptor degeneration and reduced electroretinographic responses

Mutations in myosin VIIa (MYO7A) cause Usher syndrome 1B (USH1B), a disease characterized by the combination of sensorineural hearing loss and visual impairment termed retinitis pigmentosa (RP). Although the shaker-1 mouse model of USH1B exists, only minor defects in the retina have been observed du...

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Detalhes bibliográficos
Main Authors: Wasfy, Meagan M., Matsui, Jonathan I., Miller, Jessica, Dowling, John E., Perkins, Brian D.
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4034177/
https://ncbi.nlm.nih.gov/pubmed/24698764
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.exer.2014.03.007
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