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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.

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

Ataxia3 mutant activates SCN8A. 1 / 1

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"The failure of the ataxia3 mutant to rescue the motor abnormalities and lethality of a null allele of Scn8a, together with the phenotypic similarity of ataxia3 to Scn8a mutants and the genetic mapping of ataxia3 near Scn8a, strongly support the identification of Nav1.6-S21P as the causal mutation in ataxia3 mice."

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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...