Matches in Nanopublications for { ?s ?p "[Loss-of-function mutations in SCN5A, the gene encoding Na(v)1.5 Na+ channel, are associated with inherited cardiac conduction defects and Brugada syndrome, which both exhibit variable phenotypic penetrance of conduction defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP29039.RAU5XMwipiyT2WyxkBUUrRXQnZwJpzyf5Uen8zi1NDEUg130_assertion description "[Loss-of-function mutations in SCN5A, the gene encoding Na(v)1.5 Na+ channel, are associated with inherited cardiac conduction defects and Brugada syndrome, which both exhibit variable phenotypic penetrance of conduction defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29039.RAU5XMwipiyT2WyxkBUUrRXQnZwJpzyf5Uen8zi1NDEUg130_provenance.
- assertion description "[Loss-of-function mutations in SCN5A, the gene encoding Na(v)1.5 Na+ channel, are associated with inherited cardiac conduction defects and Brugada syndrome, which both exhibit variable phenotypic penetrance of conduction defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Loss-of-function mutations in SCN5A, the gene encoding Na(v)1.5 Na+ channel, are associated with inherited cardiac conduction defects and Brugada syndrome, which both exhibit variable phenotypic penetrance of conduction defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP29150.RAPBiDZFiApdw9SKOSWoEbg_Z5qYlH_4vy0jXAWyBEX_E130_assertion description "[Loss-of-function mutations in SCN5A, the gene encoding Na(v)1.5 Na+ channel, are associated with inherited cardiac conduction defects and Brugada syndrome, which both exhibit variable phenotypic penetrance of conduction defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29150.RAPBiDZFiApdw9SKOSWoEbg_Z5qYlH_4vy0jXAWyBEX_E130_provenance.
- NP795088.RA9etodaH7SAyZfUjgFAqass3fOrMBKMsC2Ttrr0BkP28130_assertion description "[Loss-of-function mutations in SCN5A, the gene encoding Na(v)1.5 Na+ channel, are associated with inherited cardiac conduction defects and Brugada syndrome, which both exhibit variable phenotypic penetrance of conduction defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP795088.RA9etodaH7SAyZfUjgFAqass3fOrMBKMsC2Ttrr0BkP28130_provenance.