Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.
The record is no longer available at this source.
Proper Citation: RRID:MGI:5906382
Description: Allele Detail: Spontaneous This is a legacy resource.
Species: Mus musculus
Notes: Allele Detail: Spontaneous This is a legacy resource.
Phenotype: retinal cone cell degeneration, retinal rod cell degeneration, retinal degeneration, retinal photoreceptor degeneration, abnormal retinal vasculature morphology, absent visual evoked potential, abnormal eye electrophysiology, abnormal rod electrophysiology, abnormal cone electrophysiology, retinal detachment
Affected Gene: rd21
Expand AllWe found {{ ctrl2.mentions.all_count }} mentions in open access literature.
We have not found any literature mentions for this resource.
We are searching literature mentions for this resource.
Most recent articles:
{{ mention._source.dc.creators[0].familyName }} {{ mention._source.dc.creators[0].initials }}, et al. ({{ mention._source.dc.publicationYear }}) {{ mention._source.dc.title }} {{ mention._source.dc.publishers[0].name }}, {{ mention._source.dc.publishers[0].volume }}({{ mention._source.dc.publishers[0].issue }}), {{ mention._source.dc.publishers[0].pagination }}. (PMID:{{ mention._id.replace('PMID:', '') }})
A list of researchers who have used the resource and an author search tool
A list of researchers who have used the resource and an author search tool. This is available for resources that have literature mentions.
No rating or validation information has been found for rd21/rd21.
No alerts have been found for rd21/rd21.
Source: Integrated Animals
Source Database: MGI, Mouse Genome Informatics MGI