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Q33162328-1FD92832-CCEF-4460-8BCA-A4CA5E49D372
Q33162328-1FD92832-CCEF-4460-8BCA-A4CA5E49D372
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Statement
http://www.wikidata.org/entity/statement/Q33162328-1FD92832-CCEF-4460-8BCA-A4CA5E49D372
Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I(Na) contributing to LQT syndrome.
P2860
Q33162328-1FD92832-CCEF-4460-8BCA-A4CA5E49D372
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33162328-1FD92832-CCEF-4460-8BCA-A4CA5E49D372
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type
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wasDerivedFrom
276bae387b6fd9e6431d1b5922bfda9eba853dd2
P2860
GPD1L links redox state to cardiac excitability by PKC-dependent phosphorylation of the sodium channel SCN5A