Published 2010
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Early-Onset Epileptic Encephalopathy with Phospholipase C Beta 1 Deficiency
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Abstract
The clinical presentation and evolution of epileptic encephalopathy associated with a loss-of-function mutation in the phospholipase C-b 1 gene are reported in a male infant with infantile spasms treated at the University of Birmingham School of Medicine, UK.Files
PNB-24-90.pdf
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- PNB-24-90
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- Created
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2010When the item was originally created.