The PRRT2 mutation c.649dupC is the so far most frequent cause of benign familial infantile convulsions (Q46115440)
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scientific article published on 9 August 2012
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | The PRRT2 mutation c.649dupC is the so far most frequent cause of benign familial infantile convulsions |
scientific article published on 9 August 2012 |
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The PRRT2 mutation c.649dupC is the so far most frequent cause of benign familial infantile convulsions (English)
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Ortrud K Steinlein
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M Villain
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C Korenke
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9 August 2012
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21
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9
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740-742
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Identifiers
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1 reference