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Developmental and Epileptic Encephalopathy 59
A developmental and epileptic encephalopathy characterized by severe global developmental delay and onset of seizures in the first months of life that is caused by heterozygous mutation in the GABBR2 gene on chromosome 9
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Overview
A developmental and epileptic encephalopathy characterized by severe global developmental delay and onset of seizures in the first months of life that is caused by heterozygous mutation in the GABBR2 gene on chromosome 9
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