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You searched for: Author/Creator De, Peter

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1. Dominant‐negative effects of KCNQ2 mutations are associated with epileptic encephalopathy. Issue 3 (18th March 2014)

2. GRIN2B mutations in west syndrome and intellectual disability with focal epilepsy. Issue 1 (2nd January 2014)

4. Mutations in TNK2 in severe autosomal recessive infantile onset epilepsy. Issue 3 (4th September 2013)