Matches in Nanopublications for { ?s ?p "[A novel F318C substitution alters a highly conserved residue in a predicted repeat domain of LGI1 which may participate in the development of the " autosomal dominant partial epilepsy with auditory features " phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP128824.RAe3CkWgu0f0paKo1Z_ab67XhiCHWGXVeAtr5dtMgiODY130_assertion description "[A novel F318C substitution alters a highly conserved residue in a predicted repeat domain of LGI1 which may participate in the development of the " autosomal dominant partial epilepsy with auditory features " phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP128824.RAe3CkWgu0f0paKo1Z_ab67XhiCHWGXVeAtr5dtMgiODY130_provenance.
- NP199833.RABplA5_ZxyrkijA0-QKrI6EiFBSWapKw7y_4jO7QKNCg130_assertion description "[A novel F318C substitution alters a highly conserved residue in a predicted repeat domain of LGI1 which may participate in the development of the " autosomal dominant partial epilepsy with auditory features " phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199833.RABplA5_ZxyrkijA0-QKrI6EiFBSWapKw7y_4jO7QKNCg130_provenance.
- assertion description "[A novel F318C substitution alters a highly conserved residue in a predicted repeat domain of LGI1 which may participate in the development of the " autosomal dominant partial epilepsy with auditory features " phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.