Matches in Nanopublications for { ?s ?p "[Mutation screening and linkage disequilibrium mapping of the gene encoding the GABA(A) beta(3) subunit (GABRB3) identified a common genetic variant in the exon 1a promoter region (C-allele of rs4906902) which displayed a reduced transcriptional activity and showed a strong allelic association with childhood absence epilepsy (CAE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP663063.RAQWWIrdBYd3PWTzaTcYwk8Si_hmettUKej0k8tauUPk8130_assertion description "[Mutation screening and linkage disequilibrium mapping of the gene encoding the GABA(A) beta(3) subunit (GABRB3) identified a common genetic variant in the exon 1a promoter region (C-allele of rs4906902) which displayed a reduced transcriptional activity and showed a strong allelic association with childhood absence epilepsy (CAE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663063.RAQWWIrdBYd3PWTzaTcYwk8Si_hmettUKej0k8tauUPk8130_provenance.
- NP727960.RAm3KxdFAc1wzawWYEdn9yuGs0QKmUYrP6SSTCyvVv_r0130_assertion description "[Mutation screening and linkage disequilibrium mapping of the gene encoding the GABA(A) beta(3) subunit (GABRB3) identified a common genetic variant in the exon 1a promoter region (C-allele of rs4906902) which displayed a reduced transcriptional activity and showed a strong allelic association with childhood absence epilepsy (CAE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP727960.RAm3KxdFAc1wzawWYEdn9yuGs0QKmUYrP6SSTCyvVv_r0130_provenance.
- NP452098.RAhr9_F0ETEqZK567Sl-5Oi5xf1Y6R0C_9NHua1wQ8hu4130_assertion description "[Mutation screening and linkage disequilibrium mapping of the gene encoding the GABA(A) beta(3) subunit (GABRB3) identified a common genetic variant in the exon 1a promoter region (C-allele of rs4906902) which displayed a reduced transcriptional activity and showed a strong allelic association with childhood absence epilepsy (CAE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP452098.RAhr9_F0ETEqZK567Sl-5Oi5xf1Y6R0C_9NHua1wQ8hu4130_provenance.
- NP588151.RAmX1AjI4IFv1nTWlEOO3TmdzBgIIfUiVJEBfMlz8VT7U130_assertion description "[Mutation screening and linkage disequilibrium mapping of the gene encoding the GABA(A) beta(3) subunit (GABRB3) identified a common genetic variant in the exon 1a promoter region (C-allele of rs4906902) which displayed a reduced transcriptional activity and showed a strong allelic association with childhood absence epilepsy (CAE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588151.RAmX1AjI4IFv1nTWlEOO3TmdzBgIIfUiVJEBfMlz8VT7U130_provenance.
- NP889206.RA0opGR4yjK9Tfpnf-nb12oRSm22BaeI5v4xgNAFAYofA130_assertion description "[Mutation screening and linkage disequilibrium mapping of the gene encoding the GABA(A) beta(3) subunit (GABRB3) identified a common genetic variant in the exon 1a promoter region (C-allele of rs4906902) which displayed a reduced transcriptional activity and showed a strong allelic association with childhood absence epilepsy (CAE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889206.RA0opGR4yjK9Tfpnf-nb12oRSm22BaeI5v4xgNAFAYofA130_provenance.