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Article

Epilepsy: GRIN2A mutations identified as key genetic drivers of epilepsy-aphasia spectrum disorders.

Nature reviews. Neurology - 1 Oct 2013

Kingwell Katie

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 23999465
DOI: 10.1038/nrneurol.2013.181

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Whole‐exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo <i>GRIN2A</i> mutationSemantic proximity Read ↗

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Clinical phenotype and functional influence of GRIN2A variants in epilepsy-aphasia syndrome.Semantic proximity Read ↗

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Functional Evaluation of a De Novo GRIN2A Mutation Identified in a Patient with Profound Global Developmental Delay and Refractory EpilepsySemantic proximity Read ↗

Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs.Semantic proximity Read ↗

GRIN2A mutations in epilepsy-aphasia spectrum disorders.Semantic proximity Read ↗

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