Matches in Nanopublications for { ?s ?p "[L263V is the first SCN1A mutation associated with FHM and co-occurring epilepsy in multiple mutation carriers, and is the clearest molecular link between migraine and epilepsy thus far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP640175.RA_isfleCRtrzrXzY1-a-L16onVhZIaz6QjVPvvOY9K1o130_assertion description "[L263V is the first SCN1A mutation associated with FHM and co-occurring epilepsy in multiple mutation carriers, and is the clearest molecular link between migraine and epilepsy thus far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP640175.RA_isfleCRtrzrXzY1-a-L16onVhZIaz6QjVPvvOY9K1o130_provenance.
- NP720771.RAXbZpEV8vxzXHWhOK7isXQDaC4w2iGCJNqCQtTvg4S3I130_assertion description "[L263V is the first SCN1A mutation associated with FHM and co-occurring epilepsy in multiple mutation carriers, and is the clearest molecular link between migraine and epilepsy thus far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP720771.RAXbZpEV8vxzXHWhOK7isXQDaC4w2iGCJNqCQtTvg4S3I130_provenance.
- assertion description "[L263V is the first SCN1A mutation associated with FHM and co-occurring epilepsy in multiple mutation carriers, and is the clearest molecular link between migraine and epilepsy thus far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP682458.RAslkzXAo-4xFaQOn1HnjRjjKnNkMChxVOfNDIqY2AT40130_assertion description "[L263V is the first SCN1A mutation associated with FHM and co-occurring epilepsy in multiple mutation carriers, and is the clearest molecular link between migraine and epilepsy thus far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682458.RAslkzXAo-4xFaQOn1HnjRjjKnNkMChxVOfNDIqY2AT40130_provenance.