Matches in Nanopublications for { ?s ?p "[Our data associated the R349L and R190W mutations in LMNA with severe forms of familial DC. LMNA mutations should be considered in the genetic screening of patients with familial DC without conduction system disease. Isolated left ventricular noncompactio]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP69678.RAY-2mSbofzQR7xRdkeozlpAFIilb7qnkz3hh5u1wisEk130_assertion description "[Our data associated the R349L and R190W mutations in LMNA with severe forms of familial DC. LMNA mutations should be considered in the genetic screening of patients with familial DC without conduction system disease. Isolated left ventricular noncompactio]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP69678.RAY-2mSbofzQR7xRdkeozlpAFIilb7qnkz3hh5u1wisEk130_provenance.
- assertion description "[Our data associated the R349L and R190W mutations in LMNA with severe forms of familial DC. LMNA mutations should be considered in the genetic screening of patients with familial DC without conduction system disease. Isolated left ventricular noncompactio]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP86358.RAfG5MnqPbRNIRS5aT_R1z8wW-vZWi5zGslsh883MK2i0130_assertion description "[Our data associated the R349L and R190W mutations in LMNA with severe forms of familial DC. LMNA mutations should be considered in the genetic screening of patients with familial DC without conduction system disease. Isolated left ventricular noncompactio]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86358.RAfG5MnqPbRNIRS5aT_R1z8wW-vZWi5zGslsh883MK2i0130_provenance.