Matches in Nanopublications for { ?s ?p "[We report here the first dominant negative mutation in KCNQ2 that has a phenotype of neonatal seizures without permanent clinical CNS impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP844795.RANlvS56F54qzvrALgBsBztbiojD-aTh-rqnhcBoiHDCo130_assertion description "[We report here the first dominant negative mutation in KCNQ2 that has a phenotype of neonatal seizures without permanent clinical CNS impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844795.RANlvS56F54qzvrALgBsBztbiojD-aTh-rqnhcBoiHDCo130_provenance.
- assertion description "[We report here the first dominant negative mutation in KCNQ2 that has a phenotype of neonatal seizures without permanent clinical CNS impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP416146.RAY9xbTTNhCxpKjn1LIG9ZC2cu2fQVUoQVI9TcAeu8w5s130_assertion description "[We report here the first dominant negative mutation in KCNQ2 that has a phenotype of neonatal seizures without permanent clinical CNS impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP416146.RAY9xbTTNhCxpKjn1LIG9ZC2cu2fQVUoQVI9TcAeu8w5s130_provenance.