Genetics of Absence Epilepsy and Febrile Seizures
In a large family with epilepsy studied at the University of Melbourne, Australia, FS in 18 children were inherited as autosomal dominant with 75% penetrance (GABA receptor subunit mutation on chromosome 5), and absence epilepsy in 8 required the GABA gene on chromosome 5 interacting with a possible...
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Pediatric Neurology Briefs Publishers,
2003-01-01T00:00:00Z.
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