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Q33162328-5AAAA6D4-9785-4672-9748-6A7EFB4EDEA3
Q33162328-5AAAA6D4-9785-4672-9748-6A7EFB4EDEA3
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Statement
http://www.wikidata.org/entity/statement/Q33162328-5AAAA6D4-9785-4672-9748-6A7EFB4EDEA3
Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I(Na) contributing to LQT syndrome.
P2860
Q33162328-5AAAA6D4-9785-4672-9748-6A7EFB4EDEA3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33162328-5AAAA6D4-9785-4672-9748-6A7EFB4EDEA3
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wasDerivedFrom
276bae387b6fd9e6431d1b5922bfda9eba853dd2
P2860
Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24