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Omi, a recessive mutation on chromosome 10, is a novel allele of Ostm1
Large-scale N-ethyl-N-nitrosourea (ENU) mutagenesis has provided many rodent models for human disease. Here we describe the initial characterization and mapping of a recessive mutation that leads to degeneration of the incisors, failure of molars to erupt, a grey coat colour, and mild osteopetrosis....
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer-Verlag
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3560959/ https://ncbi.nlm.nih.gov/pubmed/23160729 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00335-012-9438-7 |
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