Matches in Nanopublications for { ?s ?p "[Here, we identified a novel SCN1A L263V mutation in a Portuguese family with partly co-segregating hemiplegic migraine and epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP506784.RAJT5Glou5dEYUerkZeOw6Q6HreK91D_vajpRZ5JChct4130_assertion description "[Here, we identified a novel SCN1A L263V mutation in a Portuguese family with partly co-segregating hemiplegic migraine and epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP506784.RAJT5Glou5dEYUerkZeOw6Q6HreK91D_vajpRZ5JChct4130_provenance.
- NP682479.RAY_iZujm4hNbtHrLm9437LxNLDypd_C6lnuHWsv08HuI130_assertion description "[Here, we identified a novel SCN1A L263V mutation in a Portuguese family with partly co-segregating hemiplegic migraine and epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682479.RAY_iZujm4hNbtHrLm9437LxNLDypd_C6lnuHWsv08HuI130_provenance.
- assertion description "[Here, we identified a novel SCN1A L263V mutation in a Portuguese family with partly co-segregating hemiplegic migraine and epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP720775.RANHqp77A5fx0w6iZXZFKtHYGLKnkoJfscE2QIpnNvhko130_assertion description "[Here, we identified a novel SCN1A L263V mutation in a Portuguese family with partly co-segregating hemiplegic migraine and epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP720775.RANHqp77A5fx0w6iZXZFKtHYGLKnkoJfscE2QIpnNvhko130_provenance.