Matches in Nanopublications for { ?s ?p "[We propose that familial cortical myoclonus is a novel movement disorder that may be caused by mutation in NOL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_assertion description "[We propose that familial cortical myoclonus is a novel movement disorder that may be caused by mutation in NOL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP196590.RAnjPXD3iH-9f5nr6BGebvc3QIrHNnYytgT6orPvDLwNA130_provenance.
- NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_assertion description "[We propose that familial cortical myoclonus is a novel movement disorder that may be caused by mutation in NOL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP812645.RAo4eqV8NR4n7oW6IWYXrZmJj1x_tld6X7mM9qj-6-cFA130_provenance.
- NP1008463.RAgXamw-xxnz2p7U94R4Ym7DGFkM7rjrzpPy6KdNPBTwI130_assertion description "[We propose that familial cortical myoclonus is a novel movement disorder that may be caused by mutation in NOL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1008463.RAgXamw-xxnz2p7U94R4Ym7DGFkM7rjrzpPy6KdNPBTwI130_provenance.