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PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome(legacy) 189
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome(legacy) 110

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PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome 3 11 2 1 1 5 2

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