Matches in Nanopublications for { ?s ?p "[Coexistence of unexplained ventricular hypertrophy and pre-excitation should prompt the diagnosis of PRKAG2 mutations and these patients should be referred for genetic analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP727460.RATkh65JsW_FmcjDlLxVlRcPCY7d3sm7jEFt_ihPrPo98130_assertion description "[Coexistence of unexplained ventricular hypertrophy and pre-excitation should prompt the diagnosis of PRKAG2 mutations and these patients should be referred for genetic analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP727460.RATkh65JsW_FmcjDlLxVlRcPCY7d3sm7jEFt_ihPrPo98130_provenance.
- assertion description "[Coexistence of unexplained ventricular hypertrophy and pre-excitation should prompt the diagnosis of PRKAG2 mutations and these patients should be referred for genetic analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP681402.RAIsHVNHZFfsYRbHFnJFXIcHvTvPydys7wQZUbdwl0hug130_assertion description "[Coexistence of unexplained ventricular hypertrophy and pre-excitation should prompt the diagnosis of PRKAG2 mutations and these patients should be referred for genetic analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681402.RAIsHVNHZFfsYRbHFnJFXIcHvTvPydys7wQZUbdwl0hug130_provenance.
- NP905595.RAs2B5SlMczjHg2jcFDUxWBuxAMtHAMbspzA2Hd5xn-dM130_assertion description "[Coexistence of unexplained ventricular hypertrophy and pre-excitation should prompt the diagnosis of PRKAG2 mutations and these patients should be referred for genetic analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP905595.RAs2B5SlMczjHg2jcFDUxWBuxAMtHAMbspzA2Hd5xn-dM130_provenance.
- NP550858.RA062jjYsWo0td46onFj80JO82bqm63GccFokfhbttiB8130_assertion description "[Coexistence of unexplained ventricular hypertrophy and pre-excitation should prompt the diagnosis of PRKAG2 mutations and these patients should be referred for genetic analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP550858.RA062jjYsWo0td46onFj80JO82bqm63GccFokfhbttiB8130_provenance.