Matches in Nanopublications for { ?s ?p "[We report, for a first time, a KCNQ1 mutation in a family suffering of both phenotypes, suggesting that KCNQ1 genetic variations may confer susceptibility for recurrent seizure activity increasing the risk or lead to sudden death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1260436.RAy2DhYn9yr3pejY4pKfZdruGclQ4zcdxWTsEbJ95tk7g130_assertion description "[We report, for a first time, a KCNQ1 mutation in a family suffering of both phenotypes, suggesting that KCNQ1 genetic variations may confer susceptibility for recurrent seizure activity increasing the risk or lead to sudden death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260436.RAy2DhYn9yr3pejY4pKfZdruGclQ4zcdxWTsEbJ95tk7g130_provenance.