The genetic dissection of Myo7a gene expression in the retinas of BXD mice

PURPOSE: Usher syndrome (US) is characterized by a loss of vision due to retinitis pigmentosa (RP) and deafness. US has three clinical subtypes, but even within each subtype, the severity varies. Myosin VIIA, coded by Myo7a, has been identified as one of the causal genes of US. This study aims to id...

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Detalles Bibliográficos
Autores principales: Lu, Ye, Zhou, Diana, King, Rebecca, Zhu, Shuang, Simpson, Claire L., Jones, Byron C., Zhang, Wenbo, Geisert, Eldon E., Lu, Lu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802760/
https://www.ncbi.nlm.nih.gov/pubmed/29430167

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802760/
https://www.ncbi.nlm.nih.gov/pubmed/29430167

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