De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome (Q24600816)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome |
scientific article |
Statements
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome (English)
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7 November 2013
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93
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967-75
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5
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1 reference
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1 reference