Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant mice.

Cox, G A; Lutz, C M; Yang, C L; Biemesderfer, D; Bronson, R T; Fu, A; Aronson, P S; Noebels, J L; Frankel, W N

Cox, G A; Lutz, C M; Yang, C L; Biemesderfer, D; Bronson, R T; Fu, A; Aronson, P S; Noebels, J L; Frankel, W N.

Affiliation

Cox GA; The Jackson Laboratory, Bar Harbor, Maine 04609, USA.

Cell ; 91(1): 139-48, 1997 Oct 03.

Article in En | MEDLINE | ID: mdl-9335342

Subject(s)

Epilepsy/genetics; Epilepsy/physiopathology; Mice, Neurologic Mutants/genetics; Sodium-Hydrogen Exchangers/physiology; Animals; Ataxia; Brain Chemistry; Cell Line; Cerebellum/pathology; Cerebral Cortex/physiopathology; Chromosome Mapping; Crosses, Genetic; Electroencephalography; Epilepsy/metabolism; Epilepsy/pathology; Fibroblasts; Genes, Recessive; Ion Transport; Mice; Mice, Inbred C57BL; Organ Specificity; Phenotype; Point Mutation/genetics; RNA/analysis; Sodium/metabolism; Sodium-Hydrogen Exchangers/analysis; Sodium-Hydrogen Exchangers/genetics

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Collection: 01-internacional Database: MEDLINE Main subject: Sodium-Hydrogen Exchangers / Epilepsy / Mice, Neurologic Mutants Type of study: Prognostic_studies Limits: Animals Language: En Journal: Cell Year: 1997 Type: Article Affiliation country: United States

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