Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[We also report PRRT2 mutations in five of six (83%) families affected by infantile convulsions and choreoathetosis (ICCA) syndrome, a familial syndrome in which infantile seizures and an adolescent-onset movement disorder, paroxysmal kinesigenic choreoathetosis (PKC), co-occur.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP852304.RAD92U7zFcn1Qx4sgbEp0tW7neEQqNeN0sehJuLL2nW8A130_assertion description "[We also report PRRT2 mutations in five of six (83%) families affected by infantile convulsions and choreoathetosis (ICCA) syndrome, a familial syndrome in which infantile seizures and an adolescent-onset movement disorder, paroxysmal kinesigenic choreoathetosis (PKC), co-occur.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852304.RAD92U7zFcn1Qx4sgbEp0tW7neEQqNeN0sehJuLL2nW8A130_provenance.
• NP423234.RAQD7phMuyQQZTkXxck4sAY93uF5HIeR12wiMs8zJ4clw130_assertion description "[We also report PRRT2 mutations in five of six (83%) families affected by infantile convulsions and choreoathetosis (ICCA) syndrome, a familial syndrome in which infantile seizures and an adolescent-onset movement disorder, paroxysmal kinesigenic choreoathetosis (PKC), co-occur.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP423234.RAQD7phMuyQQZTkXxck4sAY93uF5HIeR12wiMs8zJ4clw130_provenance.
• NP221402.RAO_bvAemwR3CAapnz9i1a_VrsxQ8RBqaF89oypVjFFMY130_assertion description "[We also report PRRT2 mutations in five of six (83%) families affected by infantile convulsions and choreoathetosis (ICCA) syndrome, a familial syndrome in which infantile seizures and an adolescent-onset movement disorder, paroxysmal kinesigenic choreoathetosis (PKC), co-occur.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221402.RAO_bvAemwR3CAapnz9i1a_VrsxQ8RBqaF89oypVjFFMY130_provenance.
• NP5291.RA5CEd7yaVRvYsYx-MGmzpIrYDLUyW1j7GrCNcvH4WOvc130_assertion description "[We also report PRRT2 mutations in five of six (83%) families affected by infantile convulsions and choreoathetosis (ICCA) syndrome, a familial syndrome in which infantile seizures and an adolescent-onset movement disorder, paroxysmal kinesigenic choreoathetosis (PKC), co-occur.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5291.RA5CEd7yaVRvYsYx-MGmzpIrYDLUyW1j7GrCNcvH4WOvc130_provenance.
• NP387095.RAtwE-3O2BOPEH--CSDft6I6chkkrkolKrusuqWsoB4Dc130_assertion description "[We also report PRRT2 mutations in five of six (83%) families affected by infantile convulsions and choreoathetosis (ICCA) syndrome, a familial syndrome in which infantile seizures and an adolescent-onset movement disorder, paroxysmal kinesigenic choreoathetosis (PKC), co-occur.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP387095.RAtwE-3O2BOPEH--CSDft6I6chkkrkolKrusuqWsoB4Dc130_provenance.
• NP336239.RAYXMklXePI8jBWXg1Kuvc8SAMqQhjnuBmcS0QfKEkAe8130_assertion description "[We also report PRRT2 mutations in five of six (83%) families affected by infantile convulsions and choreoathetosis (ICCA) syndrome, a familial syndrome in which infantile seizures and an adolescent-onset movement disorder, paroxysmal kinesigenic choreoathetosis (PKC), co-occur.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP336239.RAYXMklXePI8jBWXg1Kuvc8SAMqQhjnuBmcS0QfKEkAe8130_provenance.
• NP698993.RArqknAj_oPkv7Msd7O4Eknks6oClSp513uQSpCA9ZIYk130_assertion description "[We also report PRRT2 mutations in five of six (83%) families affected by infantile convulsions and choreoathetosis (ICCA) syndrome, a familial syndrome in which infantile seizures and an adolescent-onset movement disorder, paroxysmal kinesigenic choreoathetosis (PKC), co-occur.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP698993.RArqknAj_oPkv7Msd7O4Eknks6oClSp513uQSpCA9ZIYk130_provenance.
• NP616758.RAb_dud2pbiPDcF5aq0v669BNVskHNpA_ivE-RtH5_ALE130_assertion description "[We also report PRRT2 mutations in five of six (83%) families affected by infantile convulsions and choreoathetosis (ICCA) syndrome, a familial syndrome in which infantile seizures and an adolescent-onset movement disorder, paroxysmal kinesigenic choreoathetosis (PKC), co-occur.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616758.RAb_dud2pbiPDcF5aq0v669BNVskHNpA_ivE-RtH5_ALE130_provenance.
• NP6915.RATFfQDvTqaej0U_25yIFdXmOVgb845wl8mytld3YWfhk130_assertion description "[We also report PRRT2 mutations in five of six (83%) families affected by infantile convulsions and choreoathetosis (ICCA) syndrome, a familial syndrome in which infantile seizures and an adolescent-onset movement disorder, paroxysmal kinesigenic choreoathetosis (PKC), co-occur.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6915.RATFfQDvTqaej0U_25yIFdXmOVgb845wl8mytld3YWfhk130_provenance.
• assertion description "[We also report PRRT2 mutations in five of six (83%) families affected by infantile convulsions and choreoathetosis (ICCA) syndrome, a familial syndrome in which infantile seizures and an adolescent-onset movement disorder, paroxysmal kinesigenic choreoathetosis (PKC), co-occur.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We also report PRRT2 mutations in five of six (83%) families affected by infantile convulsions and choreoathetosis (ICCA) syndrome, a familial syndrome in which infantile seizures and an adolescent-onset movement disorder, paroxysmal kinesigenic choreoathetosis (PKC), co-occur.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP963766.RAIAjAmDRzRPmlD-CZmvSpH8Wna75sZctV8IbNoFSGURA130_assertion description "[We also report PRRT2 mutations in five of six (83%) families affected by infantile convulsions and choreoathetosis (ICCA) syndrome, a familial syndrome in which infantile seizures and an adolescent-onset movement disorder, paroxysmal kinesigenic choreoathetosis (PKC), co-occur.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963766.RAIAjAmDRzRPmlD-CZmvSpH8Wna75sZctV8IbNoFSGURA130_provenance.
• NP953113.RAK1MToi9nEqmPuzrhlpIA-Q08ylS4PWk8TenQ1E4PzLI130_assertion description "[We also report PRRT2 mutations in five of six (83%) families affected by infantile convulsions and choreoathetosis (ICCA) syndrome, a familial syndrome in which infantile seizures and an adolescent-onset movement disorder, paroxysmal kinesigenic choreoathetosis (PKC), co-occur.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP953113.RAK1MToi9nEqmPuzrhlpIA-Q08ylS4PWk8TenQ1E4PzLI130_provenance.