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:2429569
Description: Allele Detail: Spontaneous This is a legacy resource.
Species: Mus musculus
Notes: Allele Detail: Spontaneous This is a legacy resource.
Phenotype: motor neuron degeneration, abnormal facial nerve morphology, premature death, paralysis, abnormal phrenic nerve morphology, premature death, respiratory failure, progressive muscle weakness, axon degeneration, muscular atrophy, respiratory failure
Affected Gene: Tbce
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 Tbcepmn/Tbcepmn.
No alerts have been found for Tbcepmn/Tbcepmn.
Source: Integrated Animals
Source Database: MGI, Mouse Genome Informatics MGI