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This Service

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.

This Project

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.

IndraLab

Statements

Mutated SCN8A binds ID1. 1 / 1

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"XREF_BIBR, reported a cohort of Chinese patients and identified five de novo SCN8A variants that stated to be the first reported in Chinese patients with epilepsy and ID/DD, in our cohort we identified a novel de novo SCN8A mutation associated with unclassified EEEs and moderate ID, thus enriching the relation between SCN8A variants and EIEE."

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Our Sources:

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