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:5697875
Description: Allele Detail: Transgenic This is a legacy resource.
Species: Mus musculus
Notes: Allele Detail: Transgenic This is a legacy resource.
Phenotype: demyelination, astrocytosis, forelimb paralysis, abnormal sphingomyelin level, decreased spinal cord ventral horn cell number, decreased cholesterol level, axon degeneration, abnormal lipid level, ataxia, abnormal phospholipid level, abnormal oligodendrocyte morphology, microgliosis, premature death, abnormal motor capabilities/coordination/movement, increased oligodendrocyte number, kyphosis, abnormal spinal cord white matter morphology
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 Tg(Plp1-LMNB1)1108Qsp.
No alerts have been found for Tg(Plp1-LMNB1)1108Qsp.
Source: MGI
Source Database: MGI, Mouse Genome Informatics MGI