A novel achromatopsia mouse model resulting from a naturally occurring missense change in Cngb3
<strong>Purpose:</strong> A local colony of inbred mice (129S6/SvEvTac origin), in isolation for over a decade, were found to have absent light-adapted electroretinogram (ERG) responses. We investigated the inheritance and genetic basis of this phenotype of cone photoreceptor function lo...
主要な著者: | Hassall, M, Barnard, A, Orlans, H, McClements, M, Charbel Issa, P, Aslam, S, Maclaren, R |
---|---|
フォーマット: | Journal article |
言語: | English |
出版事項: |
Association for Research in Vision and Ophthalmology
2018
|
類似資料
-
Achromatopsia caused by novel missense mutations in the CNGA3 gene
著者:: Xi-Teng Chen, 等
出版事項: (2015-10-01) -
Correction: AAV-Mediated Cone Rescue in a Naturally Occurring Mouse Model of CNGA3-Achromatopsia
出版事項: (2014-01-01) -
Correction: AAV-Mediated Cone Rescue in a Naturally Occurring Mouse Model of CNGA3-Achromatopsia.
著者:: Ji-jing Pang, 等
出版事項: (2014-01-01) -
Inclusion of the woodchuck hepatitis virus posttranscriptional regulatory element enhances AAV2-driven transduction of mouse and human retina
著者:: Patrício, M, 等
出版事項: (2017) -
Deep phenotyping of the Cdhr1−/− mouse validates its use in pre-clinical studies for human CDHR1-associated retinal degeneration
著者:: Yusuf, I, 等
出版事項: (2021)