Early-Onset Epileptic Encephalopathy with Phospholipase C Beta 1 Deficiency
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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| Format: | Book |
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Pediatric Neurology Briefs Publishers,
2010-12-01T00:00:00Z.
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