Matches in Nanopublications for { ?s ?p "[Screening all exons of CPA6 in unrelated patients with partial epilepsy (n = 195) and FS (n = 145) revealed a new heterozygous missense mutation c.799G>A (p.Gly267Arg) in three TLE patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP927797.RAsQ0lh7nbP03Yttk6sO88Ix_CGWRk1XMxMMa84iwNoLU130_assertion description "[Screening all exons of CPA6 in unrelated patients with partial epilepsy (n = 195) and FS (n = 145) revealed a new heterozygous missense mutation c.799G>A (p.Gly267Arg) in three TLE patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927797.RAsQ0lh7nbP03Yttk6sO88Ix_CGWRk1XMxMMa84iwNoLU130_provenance.
- assertion description "[Screening all exons of CPA6 in unrelated patients with partial epilepsy (n = 195) and FS (n = 145) revealed a new heterozygous missense mutation c.799G>A (p.Gly267Arg) in three TLE patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP924295.RAjGH2p9c-SgJ22W-VRFLbkdQFWvEOhTia6yX8AjuGE30130_assertion description "[Screening all exons of CPA6 in unrelated patients with partial epilepsy (n = 195) and FS (n = 145) revealed a new heterozygous missense mutation c.799G>A (p.Gly267Arg) in three TLE patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924295.RAjGH2p9c-SgJ22W-VRFLbkdQFWvEOhTia6yX8AjuGE30130_provenance.