| Literature DB >> 2961926 |
H Höger1, J Gialamas, D Adamiker.
Abstract
A new mutation, affecting skin and hair, occurred in an expansion colony of Him:OF1 mice. Test crosses showed that a single autosomal recessive gene was responsible for this trait. Homozygotes have sparse greasy fur and lower viability and fertility than normal littermates. Histological observations showed hypertrophy of sebaceous glands, hyperkeratosis, parakeratosis, acanthosis and signs of inflammation. The disease was named 'inherited seborrheic dermatitis' and the gene name seb is proposed.Entities:
Mesh:
Year: 1987 PMID: 2961926 DOI: 10.1258/002367787781363336
Source DB: PubMed Journal: Lab Anim ISSN: 0023-6772 Impact factor: 2.471