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Q33161775-D43AC9BC-08CD-4F96-8F1D-CB7D9D1AEA68
Q33161775-D43AC9BC-08CD-4F96-8F1D-CB7D9D1AEA68
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33161775-D43AC9BC-08CD-4F96-8F1D-CB7D9D1AEA68
Inherited long QT syndrome: clinical manifestation, genetic diagnostics, and therapy.
P2860
Q33161775-D43AC9BC-08CD-4F96-8F1D-CB7D9D1AEA68
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33161775-D43AC9BC-08CD-4F96-8F1D-CB7D9D1AEA68
rank
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type
BestRank
Statement
wasDerivedFrom
bd0a3b518bdaabcaaefa590ce5df3c0f90d0379d
P2860
Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation.