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- NP1242291.RAy3JSx7MjjJ32Jc2K-rdi-DivevXmQqYW0z-dxLE1wmc130_assertion type Assertion NP1242291.RAy3JSx7MjjJ32Jc2K-rdi-DivevXmQqYW0z-dxLE1wmc130_head.
- NP1242291.RAy3JSx7MjjJ32Jc2K-rdi-DivevXmQqYW0z-dxLE1wmc130_assertion description "[ATP1A3 mutation analysis is appropriate to consider in the diagnostic algorithm for any child presenting with episodic or fluctuating ataxia, weakness or dystonia whether they manifest persistence of neurological symptoms between episodes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242291.RAy3JSx7MjjJ32Jc2K-rdi-DivevXmQqYW0z-dxLE1wmc130_provenance.
- NP1242291.RAy3JSx7MjjJ32Jc2K-rdi-DivevXmQqYW0z-dxLE1wmc130_assertion evidence source_evidence_literature NP1242291.RAy3JSx7MjjJ32Jc2K-rdi-DivevXmQqYW0z-dxLE1wmc130_provenance.
- NP1242291.RAy3JSx7MjjJ32Jc2K-rdi-DivevXmQqYW0z-dxLE1wmc130_assertion SIO_000772 25447930 NP1242291.RAy3JSx7MjjJ32Jc2K-rdi-DivevXmQqYW0z-dxLE1wmc130_provenance.
- NP1242291.RAy3JSx7MjjJ32Jc2K-rdi-DivevXmQqYW0z-dxLE1wmc130_assertion wasDerivedFrom befree-2016 NP1242291.RAy3JSx7MjjJ32Jc2K-rdi-DivevXmQqYW0z-dxLE1wmc130_provenance.
- NP1242291.RAy3JSx7MjjJ32Jc2K-rdi-DivevXmQqYW0z-dxLE1wmc130_assertion wasGeneratedBy ECO_0000203 NP1242291.RAy3JSx7MjjJ32Jc2K-rdi-DivevXmQqYW0z-dxLE1wmc130_provenance.