Published 2010 | Version v1.0.0
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Early-Onset Epileptic Encephalopathy with Phospholipase C Beta 1 Deficiency

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.

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PNB-24-90

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Created
2010
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