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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Hlavní autoři: Bosman, Erika A., Estabel, Jeanne, Ismail, Ozama, Podrini, Christine, White, Jacqueline K., Steel, Karen P.
Médium: Artigo
Jazyk:Inglês
Vydáno: Springer-Verlag 2012
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On-line přístup: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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