Article
Omi, a recessive mutation on chromosome 10, is a novel allele of Ostm1.
Mammalian genome : official journal of the International Mammalian Genome Society - 1 Feb 2013
Bosman Erika A, Estabel Jeanne, Ismail Ozama, Podrini Christine, White Jacqueline K, Steel Karen P
Abstract excerpt
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. We mapped the omi mutation to chromosome 10 between D10Mit214 and D10Mit194. The Ostm1 gene is a likely candidate...
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