Results
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17121.
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17131.
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17132.
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17133.
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17134.
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Epilepsy as part of the phenotype associated with ATP1A2 mutations. [electronic resource] by
- Deprez, Liesbet
- Weckhuysen, Sarah
- Peeters, Katelijne
- Deconinck, Tine
- Claeys, Kristl G
- Claes, Lieve R F
- Suls, Arvid
- Van Dyck, Tine
- Palmini, André
- Matthijs, Gert
- Van Paesschen, Wim
- De Jonghe, Peter
Producer: 20080611
In:
Epilepsia vol. 49
Availability: No items available.
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17135.
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17136.
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17137.
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17138.
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