Matches in Nanopublications for { ?s ?p "[We identified two heterozygous KCNJ10 mutations (p.R18Q and p.V84M) in three children (two unrelated families) with seizures, ASD, and intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP917518.RAzvg6CFl3t_M8U15pMvOMmxCpAcX6nenmA4D1AK1TZKo130_assertion description "[We identified two heterozygous KCNJ10 mutations (p.R18Q and p.V84M) in three children (two unrelated families) with seizures, ASD, and intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917518.RAzvg6CFl3t_M8U15pMvOMmxCpAcX6nenmA4D1AK1TZKo130_provenance.
- assertion description "[We identified two heterozygous KCNJ10 mutations (p.R18Q and p.V84M) in three children (two unrelated families) with seizures, ASD, and intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[We identified two heterozygous KCNJ10 mutations (p.R18Q and p.V84M) in three children (two unrelated families) with seizures, ASD, and intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP522610.RAnlV7l3n8xEEh35-lC5pS8C8n-noL_VajktZ4M9r3R70130_assertion description "[We identified two heterozygous KCNJ10 mutations (p.R18Q and p.V84M) in three children (two unrelated families) with seizures, ASD, and intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522610.RAnlV7l3n8xEEh35-lC5pS8C8n-noL_VajktZ4M9r3R70130_provenance.
- NP884056.RAh1IlNnqyGpKaLKAYzK5_sTpFdzTJnjiG23Y4QNDH348130_assertion description "[We identified two heterozygous KCNJ10 mutations (p.R18Q and p.V84M) in three children (two unrelated families) with seizures, ASD, and intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP884056.RAh1IlNnqyGpKaLKAYzK5_sTpFdzTJnjiG23Y4QNDH348130_provenance.
- NP522571.RA9AEP51bOxBe4uHj1QiqcGpHUp4jl2mHGBe-VT1I7lF8130_assertion description "[We identified two heterozygous KCNJ10 mutations (p.R18Q and p.V84M) in three children (two unrelated families) with seizures, ASD, and intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522571.RA9AEP51bOxBe4uHj1QiqcGpHUp4jl2mHGBe-VT1I7lF8130_provenance.
- NP884059.RAxCZCj1T3yav7hcgzKDZg3H7O1w7eZ28t2pIaSLo1eHQ130_assertion description "[We identified two heterozygous KCNJ10 mutations (p.R18Q and p.V84M) in three children (two unrelated families) with seizures, ASD, and intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP884059.RAxCZCj1T3yav7hcgzKDZg3H7O1w7eZ28t2pIaSLo1eHQ130_provenance.