Matches in Nanopublications for { ?s ?p "[Genetic studies have identified four forms of congenital long QT syndrome (LQTS) caused by mutations in ion channel genes located on chromosomes 3 (LQT3), 7 (LQT2), 11 (LQT1), and 21 (LQT5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP228193.RACqyyl0jgL3M_ld733b-SHs4H6kKhwl7UzXg44WjUMlo130_assertion description "[Genetic studies have identified four forms of congenital long QT syndrome (LQTS) caused by mutations in ion channel genes located on chromosomes 3 (LQT3), 7 (LQT2), 11 (LQT1), and 21 (LQT5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP228193.RACqyyl0jgL3M_ld733b-SHs4H6kKhwl7UzXg44WjUMlo130_provenance.
- NP493721.RA4aPs9xASqZY4VoM9SVsrV1UqqpVljeRaWvzi1rB5qmY130_assertion description "[Genetic studies have identified four forms of congenital long QT syndrome (LQTS) caused by mutations in ion channel genes located on chromosomes 3 (LQT3), 7 (LQT2), 11 (LQT1), and 21 (LQT5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP493721.RA4aPs9xASqZY4VoM9SVsrV1UqqpVljeRaWvzi1rB5qmY130_provenance.
- NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_assertion description "[Genetic studies have identified four forms of congenital long QT syndrome (LQTS) caused by mutations in ion channel genes located on chromosomes 3 (LQT3), 7 (LQT2), 11 (LQT1), and 21 (LQT5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_provenance.
- NP276029.RAAudwufLhpu63lD-b7-PKhYBAG2R3yt8M2J7cgQWQptA130_assertion description "[Genetic studies have identified four forms of congenital long QT syndrome (LQTS) caused by mutations in ion channel genes located on chromosomes 3 (LQT3), 7 (LQT2), 11 (LQT1), and 21 (LQT5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276029.RAAudwufLhpu63lD-b7-PKhYBAG2R3yt8M2J7cgQWQptA130_provenance.
- NP521634.RAn6ftKYjYtwwox_DRtpyn_CDtfLFEQRxsptnH3BvIL0U130_assertion description "[Genetic studies have identified four forms of congenital long QT syndrome (LQTS) caused by mutations in ion channel genes located on chromosomes 3 (LQT3), 7 (LQT2), 11 (LQT1), and 21 (LQT5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521634.RAn6ftKYjYtwwox_DRtpyn_CDtfLFEQRxsptnH3BvIL0U130_provenance.
- NP276023.RAns3N2H05lzKVIPTZrhO9g_-mYlbrdZ6CkpWWYzDeIYc130_assertion description "[Genetic studies have identified four forms of congenital long QT syndrome (LQTS) caused by mutations in ion channel genes located on chromosomes 3 (LQT3), 7 (LQT2), 11 (LQT1), and 21 (LQT5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276023.RAns3N2H05lzKVIPTZrhO9g_-mYlbrdZ6CkpWWYzDeIYc130_provenance.
- NP276024.RAt8YI8HDPaSMboGB6sNNRsZcN2EHnSrJq61Pi1H3NNFg130_assertion description "[Genetic studies have identified four forms of congenital long QT syndrome (LQTS) caused by mutations in ion channel genes located on chromosomes 3 (LQT3), 7 (LQT2), 11 (LQT1), and 21 (LQT5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276024.RAt8YI8HDPaSMboGB6sNNRsZcN2EHnSrJq61Pi1H3NNFg130_provenance.
- NP276027.RAthNaOWo6ZT5udexwvBqymJzztsXT_LcEVfRLKZTow00130_assertion description "[Genetic studies have identified four forms of congenital long QT syndrome (LQTS) caused by mutations in ion channel genes located on chromosomes 3 (LQT3), 7 (LQT2), 11 (LQT1), and 21 (LQT5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276027.RAthNaOWo6ZT5udexwvBqymJzztsXT_LcEVfRLKZTow00130_provenance.
- NP834151.RA6eGx3w8-Cydt7O9SyogScNYHKZsf7G9m81iiYuXyVGo130_assertion description "[Genetic studies have identified four forms of congenital long QT syndrome (LQTS) caused by mutations in ion channel genes located on chromosomes 3 (LQT3), 7 (LQT2), 11 (LQT1), and 21 (LQT5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP834151.RA6eGx3w8-Cydt7O9SyogScNYHKZsf7G9m81iiYuXyVGo130_provenance.
- NP276030.RA1zeylRKuuhG0T_-LPDqPjgfXsXN7NvawjUNf_VOODNo130_assertion description "[Genetic studies have identified four forms of congenital long QT syndrome (LQTS) caused by mutations in ion channel genes located on chromosomes 3 (LQT3), 7 (LQT2), 11 (LQT1), and 21 (LQT5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276030.RA1zeylRKuuhG0T_-LPDqPjgfXsXN7NvawjUNf_VOODNo130_provenance.