Matches in Nanopublications for { ?s ?p "[We have analysed the frequency of PRRT2 mutations in families with benign familial infantile convulsions without paroxysmal kinesigenic dyskinesia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP609267.RA8SZsVCUkB15RXTEOE1CUbxSoa3ra6mJ_Lc-KQTWWbhg130_assertion description "[We have analysed the frequency of PRRT2 mutations in families with benign familial infantile convulsions without paroxysmal kinesigenic dyskinesia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609267.RA8SZsVCUkB15RXTEOE1CUbxSoa3ra6mJ_Lc-KQTWWbhg130_provenance.
- assertion description "[We have analysed the frequency of PRRT2 mutations in families with benign familial infantile convulsions without paroxysmal kinesigenic dyskinesia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1003935.RAoyahBOqKeL6naILHA4Dr2pCkxFrTZaRsibOHmyh8_JQ130_assertion description "[We have analysed the frequency of PRRT2 mutations in families with benign familial infantile convulsions without paroxysmal kinesigenic dyskinesia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1003935.RAoyahBOqKeL6naILHA4Dr2pCkxFrTZaRsibOHmyh8_JQ130_provenance.