Matches in Nanopublications for { ?s ?p "[We here present a detailed functional analysis of Na(v)1.2 mutant, R1312T, which was originally found in a child with Dravet syndrome (formerly known as severe myoclonic epilepsy of infancy or SMEI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP241352.RAyQE3r2YZoZZcyKZg0vbdQaeE6xKdd_9TJK40jcaEiyY130_assertion description "[We here present a detailed functional analysis of Na(v)1.2 mutant, R1312T, which was originally found in a child with Dravet syndrome (formerly known as severe myoclonic epilepsy of infancy or SMEI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP241352.RAyQE3r2YZoZZcyKZg0vbdQaeE6xKdd_9TJK40jcaEiyY130_provenance.
- assertion description "[We here present a detailed functional analysis of Na(v)1.2 mutant, R1312T, which was originally found in a child with Dravet syndrome (formerly known as severe myoclonic epilepsy of infancy or SMEI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP988063.RAQxgl2toIAPCjyT0OoSzsoXGUmFp-io8Okbp3wCE4rE4130_assertion description "[We here present a detailed functional analysis of Na(v)1.2 mutant, R1312T, which was originally found in a child with Dravet syndrome (formerly known as severe myoclonic epilepsy of infancy or SMEI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988063.RAQxgl2toIAPCjyT0OoSzsoXGUmFp-io8Okbp3wCE4rE4130_provenance.