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Q38997049-BB8778D9-BF49-410F-876B-618E4AEE4FC9
Q38997049-BB8778D9-BF49-410F-876B-618E4AEE4FC9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38997049-BB8778D9-BF49-410F-876B-618E4AEE4FC9
Molecular Pathophysiology of Congenital Long QT Syndrome.
P2860
Q38997049-BB8778D9-BF49-410F-876B-618E4AEE4FC9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38997049-BB8778D9-BF49-410F-876B-618E4AEE4FC9
rank
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type
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Statement
wasDerivedFrom
308e96690b0db03643661f90410088778f5bd4b5
P2860
Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation.