Matches in Nanopublications for { ?s ?p "[Mutations in KCNT1 were found in two seemingly unrelated monogenic epilepsies including malignant migrating partial seizures of infancy and severe autosomal dominant nocturnal frontal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP810211.RAa6ZR-atf8Tivr76oBF7xQf3xXJBn7OSMUpdQbRedIuQ130_assertion description "[Mutations in KCNT1 were found in two seemingly unrelated monogenic epilepsies including malignant migrating partial seizures of infancy and severe autosomal dominant nocturnal frontal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810211.RAa6ZR-atf8Tivr76oBF7xQf3xXJBn7OSMUpdQbRedIuQ130_provenance.
- NP817001.RAcKAG91vzKwU3U9h01khD0gxqWtGoDir_0DUxMQ2KgEA130_assertion description "[Mutations in KCNT1 were found in two seemingly unrelated monogenic epilepsies including malignant migrating partial seizures of infancy and severe autosomal dominant nocturnal frontal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817001.RAcKAG91vzKwU3U9h01khD0gxqWtGoDir_0DUxMQ2KgEA130_provenance.
- NP686607.RAT0RCY_Ige4jMmdSYC6BTRVX0Vfmu40i-MAzMOROHw6k130_assertion description "[Mutations in KCNT1 were found in two seemingly unrelated monogenic epilepsies including malignant migrating partial seizures of infancy and severe autosomal dominant nocturnal frontal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP686607.RAT0RCY_Ige4jMmdSYC6BTRVX0Vfmu40i-MAzMOROHw6k130_provenance.
- NP932189.RAeVUQwuoAcKm8XUwAubRi6mXzkLBVgfX4Gf5ONfW_o7A130_assertion description "[Mutations in KCNT1 were found in two seemingly unrelated monogenic epilepsies including malignant migrating partial seizures of infancy and severe autosomal dominant nocturnal frontal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932189.RAeVUQwuoAcKm8XUwAubRi6mXzkLBVgfX4Gf5ONfW_o7A130_provenance.
- assertion description "[Mutations in KCNT1 were found in two seemingly unrelated monogenic epilepsies including malignant migrating partial seizures of infancy and severe autosomal dominant nocturnal frontal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in KCNT1 were found in two seemingly unrelated monogenic epilepsies including malignant migrating partial seizures of infancy and severe autosomal dominant nocturnal frontal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in KCNT1 were found in two seemingly unrelated monogenic epilepsies including malignant migrating partial seizures of infancy and severe autosomal dominant nocturnal frontal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP932194.RAr8HAGsbEqkZcxd81i6nMqic6RwbRmOKPyJvxs19rVbI130_assertion description "[Mutations in KCNT1 were found in two seemingly unrelated monogenic epilepsies including malignant migrating partial seizures of infancy and severe autosomal dominant nocturnal frontal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932194.RAr8HAGsbEqkZcxd81i6nMqic6RwbRmOKPyJvxs19rVbI130_provenance.
- NP932198.RADjL-FJ5ct-nicTiQFYurlG_K6fOCLH1nnmQuFXwbrzo130_assertion description "[Mutations in KCNT1 were found in two seemingly unrelated monogenic epilepsies including malignant migrating partial seizures of infancy and severe autosomal dominant nocturnal frontal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932198.RADjL-FJ5ct-nicTiQFYurlG_K6fOCLH1nnmQuFXwbrzo130_provenance.
- NP1054800.RAlO3QlZ8UjZA6-a9dN7Ei2o6mXrac6Tu2HNq_b5OPVJ4130_assertion description "[Mutations in KCNT1 were found in two seemingly unrelated monogenic epilepsies including malignant migrating partial seizures of infancy and severe autosomal dominant nocturnal frontal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1054800.RAlO3QlZ8UjZA6-a9dN7Ei2o6mXrac6Tu2HNq_b5OPVJ4130_provenance.
- NP1054803.RAG1zh5A4V0koxC6Zdh6SvjwK7I1sJYoSpQD8GJIw3wBA130_assertion description "[Mutations in KCNT1 were found in two seemingly unrelated monogenic epilepsies including malignant migrating partial seizures of infancy and severe autosomal dominant nocturnal frontal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1054803.RAG1zh5A4V0koxC6Zdh6SvjwK7I1sJYoSpQD8GJIw3wBA130_provenance.
- NP1054802.RA4alEWa5-nXYvAy-YPQH5ii8XnXGXEi9TiNMwRcbCq0c130_assertion description "[Mutations in KCNT1 were found in two seemingly unrelated monogenic epilepsies including malignant migrating partial seizures of infancy and severe autosomal dominant nocturnal frontal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1054802.RA4alEWa5-nXYvAy-YPQH5ii8XnXGXEi9TiNMwRcbCq0c130_provenance.