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A database built with INDRA combining content from numerous readers and databases. This page allows you to curate the loaded statements. For more information please see the manual.

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INDRA is developed by indralabs, a part of the Harvard Medical School Laboratory of Systems Pharmacology.

This project, indra_db, is also developed by the indralab team. For more information on how we procure our sources, you can go here. This work was funded by ARO grant W911NF‐15‐1‐0544 under the DARPA Communicating with Computers program.

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Statements

SCN5A binds BS. 3 / 3

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"To date, 119 SCN5A mutations have been associated with BS ( Fig. 2 )."

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"Mutations in SCN5A associated with the BS phenotype usually result in a loss of channel function by a reduction in Na+ currents."

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"Mutation R1193Q has been associated with both LQT3 and BS in the French Canadian population ( Huang et al., 2006 )."

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INDRA allows us to combine the results from a multitude of sources. In particular, the INDRA Database draws on the following...

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Statements

SCN5A binds BS. 3 / 3

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