Matches in Nanopublications for { ?s ?p "[Mutations in the PRRT2 gene have been recently described as a cause of paroxysmal kinesigenic dyskinesia, infantile convulsions with choreoathetosis syndrome and, less often, infantile convulsions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP723915.RAVAkVrErjz9TqQT0KM_4f8fdfccrFZlNmQ0jH_ML9zVk130_assertion description "[Mutations in the PRRT2 gene have been recently described as a cause of paroxysmal kinesigenic dyskinesia, infantile convulsions with choreoathetosis syndrome and, less often, infantile convulsions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723915.RAVAkVrErjz9TqQT0KM_4f8fdfccrFZlNmQ0jH_ML9zVk130_provenance.