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[해외논문] Absence Epilepsy in Tottering Mutant Mice Is Associated with Calcium Channel Defects 원문보기

Cell, v.87 no.4, 1996년, pp.607 - 617  

Fletcher, Colin F (Mammalian Genetics Laboratory, ABL–) ,  Lutz, Cathleen M (Basic Research Program, NCI–) ,  O'Sullivan, T.Norene (Frederick Cancer Research, and Development Center, Frederick, Maryland 21702, USA) ,  Shaughnessy Jr., John D (The Jackson Laboratory, Bar Harbor, Maine 04609, USA) ,  Hawkes Jr., Richard (Mammalian Genetics Laboratory, ABL–) ,  Frankel Jr., Wayne N (Basic Research Program, NCI–) ,  Copeland Jr., Neal G (Frederick Cancer Research, and Development Center, Frederick, Maryland 21702, USA) ,  Jenkins Jr., Nancy A (Mammalian Genetics Laboratory, ABL–)

Abstract AI-Helper 아이콘AI-Helper

AbstractMutations at the mouse tottering (tg) locus cause a delayed-onset, recessive neurological disorder resulting in ataxia, motor seizures, and behavioral absence seizures resembling petit mal epilepsy in humans. A more severe allele, leaner (tgla), also shows a slow, selective degeneration of c...

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