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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- NP559171.RAU8Eiu10QTRzbpz0gVqBp_467QVCPpFGcNDW-H8y2Myo130_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." NP559171.RAU8Eiu10QTRzbpz0gVqBp_467QVCPpFGcNDW-H8y2Myo130_provenance.
- NP900550.RAPZRf1fjpMsc6rS0iLMFGZqobWaln_UpKzTk7poYhm2Q130_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." NP900550.RAPZRf1fjpMsc6rS0iLMFGZqobWaln_UpKzTk7poYhm2Q130_provenance.