Matches in Nanopublications for { ?s ?p "[To report the identification of the T1174S SCN1A (NaV 1.1) mutation in a three-generation family with both epileptic and familial hemiplegic migraine (FHM) phenotypes and clarify the pathomechanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP540177.RAxgZS3QOcyX_Fp9ZqD7q8QCma0fEyZym8SjkzXdAFX8M130_assertion description "[To report the identification of the T1174S SCN1A (NaV 1.1) mutation in a three-generation family with both epileptic and familial hemiplegic migraine (FHM) phenotypes and clarify the pathomechanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540177.RAxgZS3QOcyX_Fp9ZqD7q8QCma0fEyZym8SjkzXdAFX8M130_provenance.
- assertion description "[To report the identification of the T1174S SCN1A (NaV 1.1) mutation in a three-generation family with both epileptic and familial hemiplegic migraine (FHM) phenotypes and clarify the pathomechanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[To report the identification of the T1174S SCN1A (NaV 1.1) mutation in a three-generation family with both epileptic and familial hemiplegic migraine (FHM) phenotypes and clarify the pathomechanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[To report the identification of the T1174S SCN1A (NaV 1.1) mutation in a three-generation family with both epileptic and familial hemiplegic migraine (FHM) phenotypes and clarify the pathomechanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1051812.RAdnSQKJCJf4qzJkaFp6tXabBrY145p6om-qvMU5h1lGU130_assertion description "[To report the identification of the T1174S SCN1A (NaV 1.1) mutation in a three-generation family with both epileptic and familial hemiplegic migraine (FHM) phenotypes and clarify the pathomechanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1051812.RAdnSQKJCJf4qzJkaFp6tXabBrY145p6om-qvMU5h1lGU130_provenance.
- NP1051815.RAbwVVKEt7S4oHQH17mr3ldQIiX7BzJ1hFX3V8RWG7Z2Q130_assertion description "[To report the identification of the T1174S SCN1A (NaV 1.1) mutation in a three-generation family with both epileptic and familial hemiplegic migraine (FHM) phenotypes and clarify the pathomechanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1051815.RAbwVVKEt7S4oHQH17mr3ldQIiX7BzJ1hFX3V8RWG7Z2Q130_provenance.
- NP1051813.RAtlfH6eGxvaqR7oZsC-gAYmmX6SoiadXeFfhhUWWqDuU130_assertion description "[To report the identification of the T1174S SCN1A (NaV 1.1) mutation in a three-generation family with both epileptic and familial hemiplegic migraine (FHM) phenotypes and clarify the pathomechanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1051813.RAtlfH6eGxvaqR7oZsC-gAYmmX6SoiadXeFfhhUWWqDuU130_provenance.
- NP682596.RALKMdbpZDS3sXEfYxO18nVK2nUB4D--CMJR0cmW60l30130_assertion description "[To report the identification of the T1174S SCN1A (NaV 1.1) mutation in a three-generation family with both epileptic and familial hemiplegic migraine (FHM) phenotypes and clarify the pathomechanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682596.RALKMdbpZDS3sXEfYxO18nVK2nUB4D--CMJR0cmW60l30130_provenance.
- NP682492.RA15J37c9e2yadakhlQhMkQc9J_HuBJazi53BLsh1Nkos130_assertion description "[To report the identification of the T1174S SCN1A (NaV 1.1) mutation in a three-generation family with both epileptic and familial hemiplegic migraine (FHM) phenotypes and clarify the pathomechanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682492.RA15J37c9e2yadakhlQhMkQc9J_HuBJazi53BLsh1Nkos130_provenance.