Matches in Nanopublications for { ?s ?p "[The present study is the first to report mutations in GPD1-L as a pathogenic cause for a small subset of sudden infant death syndrome via a secondary loss-of-function mechanism whereby perturbations in GPD1-L precipitate a marked decrease in the peak sodium current and a potentially lethal BrS-like proarrhythmic substrate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP313051.RAu-v4Or9AW1AqnA5OivBaYqrWCqe-3K6-LCRMIzaq4C8130_assertion description "[The present study is the first to report mutations in GPD1-L as a pathogenic cause for a small subset of sudden infant death syndrome via a secondary loss-of-function mechanism whereby perturbations in GPD1-L precipitate a marked decrease in the peak sodium current and a potentially lethal BrS-like proarrhythmic substrate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP313051.RAu-v4Or9AW1AqnA5OivBaYqrWCqe-3K6-LCRMIzaq4C8130_provenance.
- NP270423.RAkRTB-tyk8Ojc-pu2pEl6K6gLBcWvbyhgbfYVBrOnOhw130_assertion description "[The present study is the first to report mutations in GPD1-L as a pathogenic cause for a small subset of sudden infant death syndrome via a secondary loss-of-function mechanism whereby perturbations in GPD1-L precipitate a marked decrease in the peak sodium current and a potentially lethal BrS-like proarrhythmic substrate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP270423.RAkRTB-tyk8Ojc-pu2pEl6K6gLBcWvbyhgbfYVBrOnOhw130_provenance.
- NP869616.RARsQBj7OwIeeF1K6rzK6yfLc16qiPeOj7LC0VRpwO_ec130_assertion description "[The present study is the first to report mutations in GPD1-L as a pathogenic cause for a small subset of sudden infant death syndrome via a secondary loss-of-function mechanism whereby perturbations in GPD1-L precipitate a marked decrease in the peak sodium current and a potentially lethal BrS-like proarrhythmic substrate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869616.RARsQBj7OwIeeF1K6rzK6yfLc16qiPeOj7LC0VRpwO_ec130_provenance.
- assertion description "[The present study is the first to report mutations in GPD1-L as a pathogenic cause for a small subset of sudden infant death syndrome via a secondary loss-of-function mechanism whereby perturbations in GPD1-L precipitate a marked decrease in the peak sodium current and a potentially lethal BrS-like proarrhythmic substrate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP637583.RALFGyRvXv344fvlezLSttbmrWdbq-86Jt_sZLQiWeFuY130_assertion description "[The present study is the first to report mutations in GPD1-L as a pathogenic cause for a small subset of sudden infant death syndrome via a secondary loss-of-function mechanism whereby perturbations in GPD1-L precipitate a marked decrease in the peak sodium current and a potentially lethal BrS-like proarrhythmic substrate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP637583.RALFGyRvXv344fvlezLSttbmrWdbq-86Jt_sZLQiWeFuY130_provenance.