Matches in Nanopublications for { ?s ?p "[Mutations in CACNA1C that increase current through the CaV1.2 L-type Ca2+ channel underlie rare forms of long QT syndrome (LQTS), and Timothy syndrome (TS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Mutations in CACNA1C that increase current through the CaV1.2 L-type Ca2+ channel underlie rare forms of long QT syndrome (LQTS), and Timothy syndrome (TS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in CACNA1C that increase current through the CaV1.2 L-type Ca2+ channel underlie rare forms of long QT syndrome (LQTS), and Timothy syndrome (TS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1216432.RAQuASdIxowYw2IX50qBkZQPdp1OuLOsSb3uDxIOdCcbU130_assertion description "[Mutations in CACNA1C that increase current through the CaV1.2 L-type Ca2+ channel underlie rare forms of long QT syndrome (LQTS), and Timothy syndrome (TS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216432.RAQuASdIxowYw2IX50qBkZQPdp1OuLOsSb3uDxIOdCcbU130_provenance.
- NP1216433.RAHUDwxnzFmWOrxbUZFwoCYztCWSBEriCMeumBwm2hPT4130_assertion description "[Mutations in CACNA1C that increase current through the CaV1.2 L-type Ca2+ channel underlie rare forms of long QT syndrome (LQTS), and Timothy syndrome (TS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216433.RAHUDwxnzFmWOrxbUZFwoCYztCWSBEriCMeumBwm2hPT4130_provenance.