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Your search keyword '"Regan, BM"' showing total 6 results

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1. High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.

2. De Novo Mutations in PPP3CA Cause Severe Neurodevelopmental Disease with Seizures.

3. A targeted resequencing gene panel for focal epilepsy.

4. Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations.

5. GRIN2A mutations cause epilepsy-aphasia spectrum disorders.

6. Mutations in DEPDC5 cause familial focal epilepsy with variable foci.

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