Matches in Nanopublications for { ?s ?p "[Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP324877.RACAs-CFHTsvYzh5EsHymQhDTmfrZN7addszUfJbtuMnE130_assertion description "[Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324877.RACAs-CFHTsvYzh5EsHymQhDTmfrZN7addszUfJbtuMnE130_provenance.
- NP324878.RAA0WLOuhQfcw1XErKgg7_jp1VDlEF9m5Raukow-uLnSE130_assertion description "[Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324878.RAA0WLOuhQfcw1XErKgg7_jp1VDlEF9m5Raukow-uLnSE130_provenance.