Matches in Nanopublications for { ?s ?p "[This case indicates that the phenotypic spectrum of infantile seizures or epilepsy with PRRT2-related pathology may be larger than previously expected, and that genetic investigation of the effect of PRRT2 mutations on idiopathic seizures or epilepsy in childhood may help elucidate the pathological backgrounds of benign childhood epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1086049.RASJBa5msUsXYY-IpZnVv-VllVWYLsWHFKD0S99IMpX5U130_assertion description "[This case indicates that the phenotypic spectrum of infantile seizures or epilepsy with PRRT2-related pathology may be larger than previously expected, and that genetic investigation of the effect of PRRT2 mutations on idiopathic seizures or epilepsy in childhood may help elucidate the pathological backgrounds of benign childhood epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1086049.RASJBa5msUsXYY-IpZnVv-VllVWYLsWHFKD0S99IMpX5U130_provenance.
- NP963547.RAtRjKnty1Cl6IywEea2BSZqxOH_yW_1mEF08fmInUzM4130_assertion description "[This case indicates that the phenotypic spectrum of infantile seizures or epilepsy with PRRT2-related pathology may be larger than previously expected, and that genetic investigation of the effect of PRRT2 mutations on idiopathic seizures or epilepsy in childhood may help elucidate the pathological backgrounds of benign childhood epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963547.RAtRjKnty1Cl6IywEea2BSZqxOH_yW_1mEF08fmInUzM4130_provenance.
- NP1086050.RAJrEKXMXQUJEQH58P4eqdjcrCQVpAIOftuBVJ8TEZVOY130_assertion description "[This case indicates that the phenotypic spectrum of infantile seizures or epilepsy with PRRT2-related pathology may be larger than previously expected, and that genetic investigation of the effect of PRRT2 mutations on idiopathic seizures or epilepsy in childhood may help elucidate the pathological backgrounds of benign childhood epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1086050.RAJrEKXMXQUJEQH58P4eqdjcrCQVpAIOftuBVJ8TEZVOY130_provenance.
- NP963621.RA_072bH2r-dJyfpngo8e1SujAec4ifyKau-anRldSWVE130_assertion description "[This case indicates that the phenotypic spectrum of infantile seizures or epilepsy with PRRT2-related pathology may be larger than previously expected, and that genetic investigation of the effect of PRRT2 mutations on idiopathic seizures or epilepsy in childhood may help elucidate the pathological backgrounds of benign childhood epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963621.RA_072bH2r-dJyfpngo8e1SujAec4ifyKau-anRldSWVE130_provenance.