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Developmental and Epileptic Encephalopathy 69
A developmental and epileptic encephalopathy characterized by early-onset refractory seizures, hypotonia, and profoundly impaired development that is caused by heterozygous mutation in the CACNA1E gene on chromosome 1q25
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Overview
A developmental and epileptic encephalopathy characterized by early-onset refractory seizures, hypotonia, and profoundly impaired development that is caused by heterozygous mutation in the CACNA1E gene on chromosome 1q25
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