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Q34395488-370B31D9-0C9F-467D-8AD0-4E05916B9EFD
Q34395488-370B31D9-0C9F-467D-8AD0-4E05916B9EFD
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http://www.wikidata.org/entity/statement/Q34395488-370B31D9-0C9F-467D-8AD0-4E05916B9EFD
Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death.
P2860
Q34395488-370B31D9-0C9F-467D-8AD0-4E05916B9EFD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34395488-370B31D9-0C9F-467D-8AD0-4E05916B9EFD
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wasDerivedFrom
6f728098fba3da827363437365a95895dc38f26e
P2860
Dual variation in SCN5A and CACNB2b underlies the development of cardiac conduction disease without Brugada syndrome.