ArticleMammalian genome : official journal of the International Mammalian Genome Society1994
The stumbler mutation maps to proximal mouse chromosome 2.
Article in Mammalian genome : official journal of the International Mammalian Genome Society, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
3 citing papers in PubMed.
- Spontaneous shaker rat mutant - a new model for X-linked tremor/ataxia.Disease models & mechanisms · 2016Article
- Cell-type specific proximity of centromeric domains of one homologue each of chromosomes 2 and 11 in nuclei of cerebellar Purkinje neurons.Chromosoma · 2006Article
- New seizure frequency QTL and the complex genetics of epilepsy in EL mice.Mammalian genome : official journal of the International Mammalian Genome Society · 1995Article
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Authors and funding
3 authors.
Funding
Abstract
The cerebellar mouse mutation stumbler (stu) was mapped to proximal Chromosome (Chr) 2 with a recently developed polymerase chain reaction assay for endogenous retroviruses that vary between mouse strains. The stu locus resides between the markers D2Mit5 and D2Mit7. A number of developmentally or neurologically relevant candidate genes map in this region, including Bmi1, Dbh, Grin1, Notch1, Pax8, Rxra, and Spna2. Knowing the chromosomal localization of stu should simplify maintenance of the stumbler mouse stock and also enable analysis of the cerebellar defect in presymptomatic individuals.
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