STARGAZER - A NEW NEUROLOGICAL MUTANT ON CHROMOSOME-15 IN THE MOUSE WITH PROLONGED CORTICAL SEIZURES

被引:185
作者
NOEBELS, JL
QIAO, X
BRONSON, RT
SPENCER, C
DAVISSON, MT
机构
[1] BAYLOR UNIV,INST MOLEC GENET,HOUSTON,TX 77030
[2] JACKSON LAB,BAR HARBOR,ME 04609
关键词
Gene; Generalized spike discharge; Inherited epilepsy; Linkage mapping; Mutation; Robertsonian chromosome;
D O I
10.1016/0920-1211(90)90098-G
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We report here the initial description of the inheritance pattern, linkage mapping, and electroclinical phenotype of a recessive mutation on mouse Chromosome 15, stargazer (stg), that produces epilepsy. The salient epileptic phenotype is a syndrome of spontaneous, prolonged, generalized spike-wave cortical discharges with behavioral arrest. A second, complex, seizure pattern featuring movements during the discharge can also appear. The stg/stg mutant phenotype confirms the general principal that inherited epilepsies sharing similar cortical excitability patterns can be transmitted by single gene loci residing on different chromosomes and provides new evidence that the severity of seizure expression depends on the specific mutant gene affected. © 1990.
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页码:129 / 135
页数:7
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