Matches in Nanopublications for { ?s ?p "[This is the first study to identify a dominant mechanism, class 2, for the loss of Kv11.1 channel function in LQT2 and to report that the class 2 phenotype for many of these mutant channels can be corrected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP978030.RAPFT6eGidlcoMPNgoQtnXig4b03yMKS5SyvCWJyOpTmU130_assertion description "[This is the first study to identify a dominant mechanism, class 2, for the loss of Kv11.1 channel function in LQT2 and to report that the class 2 phenotype for many of these mutant channels can be corrected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978030.RAPFT6eGidlcoMPNgoQtnXig4b03yMKS5SyvCWJyOpTmU130_provenance.
- NP532485.RAJFkd0xceACp39TwVwWyxzSDIxETw4WQdmFbMzp_RbgQ130_assertion description "[This is the first study to identify a dominant mechanism, class 2, for the loss of Kv11.1 channel function in LQT2 and to report that the class 2 phenotype for many of these mutant channels can be corrected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532485.RAJFkd0xceACp39TwVwWyxzSDIxETw4WQdmFbMzp_RbgQ130_provenance.
- NP532484.RA5lBEvg89SH7Yklo3BV1eP_OFl-YqJgVJLcvWnJNdJjU130_assertion description "[This is the first study to identify a dominant mechanism, class 2, for the loss of Kv11.1 channel function in LQT2 and to report that the class 2 phenotype for many of these mutant channels can be corrected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532484.RA5lBEvg89SH7Yklo3BV1eP_OFl-YqJgVJLcvWnJNdJjU130_provenance.