PubMed · 1989 · 69 citations · 3 references
Life SciencesGeneticsNeuroscienceEpilepsyNeurobiology Of DiseaseNeurogeneticsDevelopmental MutationsGenetic DisordersHereditary NeuropathiesNeurodevelopmental DisordersNeurodevelopmental GeneticsNeurogenetic DisordersAtaxia SyndromesAutosomal Recessive InheritanceGenetic Basis Of TremorHereditary AtaxiasMutationNeurological EtiologySeizuresTremor Pathophysiology
A spontaneous neurological mutation was detected in a colony of Sprague Dawley rats. The animals developed a progressive neurological syndrome characterized by tremor (which appeared at the age of 1 month), ataxia (at 4 months), immobility episodes (after 5-6 months), audiogenic seizures and hindlimb paralysis (after 10 months). Cross breeding experiments indicate that this is an autosomal recessive mutation, which we have named taiep subline.
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Myelin deficiency (md): a neurologic mutant in the Wistar rat.
Csiza Ck, de Lahunta A · PubMed · 1979 · 94 citations · Full text
Medicine, Neurobiology, Neuroscience +16