Matches in Nanopublications for { ?s ?p "[Novel ATP1A2 mutations were found in two of the 20 families (10%)/p.Gly900Arg mutation was present in a family with epilepsy and FHM, and the p.Cys702Tyr mutation occurred in a family with occipitotemporal epilepsy and migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP142199.RAKRaKq40ssQVaOujBMIRQ0Wgu8dYv9tbESNc2y_MQNaw130_assertion description "[Novel ATP1A2 mutations were found in two of the 20 families (10%)/p.Gly900Arg mutation was present in a family with epilepsy and FHM, and the p.Cys702Tyr mutation occurred in a family with occipitotemporal epilepsy and migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP142199.RAKRaKq40ssQVaOujBMIRQ0Wgu8dYv9tbESNc2y_MQNaw130_provenance.
- NP127000.RAugF9P-BDHbj7li_3LxAdVkk7iEMSXppHsJF4Ta82YTY130_assertion description "[Novel ATP1A2 mutations were found in two of the 20 families (10%)/p.Gly900Arg mutation was present in a family with epilepsy and FHM, and the p.Cys702Tyr mutation occurred in a family with occipitotemporal epilepsy and migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP127000.RAugF9P-BDHbj7li_3LxAdVkk7iEMSXppHsJF4Ta82YTY130_provenance.
- assertion description "[Novel ATP1A2 mutations were found in two of the 20 families (10%)/p.Gly900Arg mutation was present in a family with epilepsy and FHM, and the p.Cys702Tyr mutation occurred in a family with occipitotemporal epilepsy and migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Novel ATP1A2 mutations were found in two of the 20 families (10%)/p.Gly900Arg mutation was present in a family with epilepsy and FHM, and the p.Cys702Tyr mutation occurred in a family with occipitotemporal epilepsy and migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP231413.RADFmCmY3XRJFvrJRdbV8GRz_2-SOQIPK5iQvkSC_ZqUg130_assertion description "[Novel ATP1A2 mutations were found in two of the 20 families (10%)/p.Gly900Arg mutation was present in a family with epilepsy and FHM, and the p.Cys702Tyr mutation occurred in a family with occipitotemporal epilepsy and migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP231413.RADFmCmY3XRJFvrJRdbV8GRz_2-SOQIPK5iQvkSC_ZqUg130_provenance.
- NP190181.RA86RoFWRrM7GhzqRUEEH4U7Y0754d7h6Bt6pV-GtfzEY130_assertion description "[Novel ATP1A2 mutations were found in two of the 20 families (10%)/p.Gly900Arg mutation was present in a family with epilepsy and FHM, and the p.Cys702Tyr mutation occurred in a family with occipitotemporal epilepsy and migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP190181.RA86RoFWRrM7GhzqRUEEH4U7Y0754d7h6Bt6pV-GtfzEY130_provenance.
- NP205342.RA1KeNSs7gPd-JGS0_9T1bwhNsmWiCbL1cNpl6Audgzm4130_assertion description "[Novel ATP1A2 mutations were found in two of the 20 families (10%)/p.Gly900Arg mutation was present in a family with epilepsy and FHM, and the p.Cys702Tyr mutation occurred in a family with occipitotemporal epilepsy and migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205342.RA1KeNSs7gPd-JGS0_9T1bwhNsmWiCbL1cNpl6Audgzm4130_provenance.
- NP231412.RA3JzlkEzd7Yk2IwBcih9fWH6sfNuNJCIGGa0w8K6beas130_assertion description "[Novel ATP1A2 mutations were found in two of the 20 families (10%)/p.Gly900Arg mutation was present in a family with epilepsy and FHM, and the p.Cys702Tyr mutation occurred in a family with occipitotemporal epilepsy and migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP231412.RA3JzlkEzd7Yk2IwBcih9fWH6sfNuNJCIGGa0w8K6beas130_provenance.