Matches in Nanopublications for { ?s ?p "[Sequencing of the LMNA exons revealed one missense mutation at C568T (Arg190Trp) in the alpha-helical rod domain of the LMNA gene co-segregating with FDC with conduction-system disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP436099.RA_VfLYLieVGJXCOSqAJBYnYULOdatmfvfRhzSVYeasew130_assertion description "[Sequencing of the LMNA exons revealed one missense mutation at C568T (Arg190Trp) in the alpha-helical rod domain of the LMNA gene co-segregating with FDC with conduction-system disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP436099.RA_VfLYLieVGJXCOSqAJBYnYULOdatmfvfRhzSVYeasew130_provenance.
- assertion description "[Sequencing of the LMNA exons revealed one missense mutation at C568T (Arg190Trp) in the alpha-helical rod domain of the LMNA gene co-segregating with FDC with conduction-system disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP596870.RAMjZar8fQ1eGNIz1XJgghgLYbim2YrdNfogV65WFJDYo130_assertion description "[Sequencing of the LMNA exons revealed one missense mutation at C568T (Arg190Trp) in the alpha-helical rod domain of the LMNA gene co-segregating with FDC with conduction-system disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP596870.RAMjZar8fQ1eGNIz1XJgghgLYbim2YrdNfogV65WFJDYo130_provenance.