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Q33161026-EB0F396A-3E56-49D6-9B20-88941B6860AE
Q33161026-EB0F396A-3E56-49D6-9B20-88941B6860AE
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Statement
http://www.wikidata.org/entity/statement/Q33161026-EB0F396A-3E56-49D6-9B20-88941B6860AE
Genetic variants in SCN5A promoter are associated with arrhythmia phenotype severity in patients with heterozygous loss-of-function mutation
P2860
Q33161026-EB0F396A-3E56-49D6-9B20-88941B6860AE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33161026-EB0F396A-3E56-49D6-9B20-88941B6860AE
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type
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wasDerivedFrom
c38120ed5d87ac82ebcaf8ec7f0f58f025dd6ca5
P2860
SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome.