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[This study shows that mutations in STXBP1 are not limited to patients with Ohtahara syndrome, but are also present in 10% (5/49) of patients with an early-onset epileptic encephalopathy that does not fit into either Ohtahara or West syndrome and rarely in typical West syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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