Matches in Nanopublications for { ?s ?p "[This novel causative mutation (D614N) within the DNM2 gene in a large Polish centronuclear myopathy family with a late age of overt clinical manifestation caused profound changes in DNM2 localization and impaired proper organization of myofibers, and skeletal muscle functioning.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP566862.RAiXWRQ9hrtdpg6GgqnM4ZcsWXMRHkN83oQKPxf47o930130_assertion description "[This novel causative mutation (D614N) within the DNM2 gene in a large Polish centronuclear myopathy family with a late age of overt clinical manifestation caused profound changes in DNM2 localization and impaired proper organization of myofibers, and skeletal muscle functioning.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP566862.RAiXWRQ9hrtdpg6GgqnM4ZcsWXMRHkN83oQKPxf47o930130_provenance.