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- NP1041596.RACN4U6hZ9r5N_DC1KzSqWFNbIazeYD7G7JhxRjLL3GYA130_assertion type Assertion NP1041596.RACN4U6hZ9r5N_DC1KzSqWFNbIazeYD7G7JhxRjLL3GYA130_head.
- NP1041596.RACN4U6hZ9r5N_DC1KzSqWFNbIazeYD7G7JhxRjLL3GYA130_assertion wasGeneratedBy ECO_0000203 NP1041596.RACN4U6hZ9r5N_DC1KzSqWFNbIazeYD7G7JhxRjLL3GYA130_provenance.
- NP1041596.RACN4U6hZ9r5N_DC1KzSqWFNbIazeYD7G7JhxRjLL3GYA130_assertion wasDerivedFrom befree-2016 NP1041596.RACN4U6hZ9r5N_DC1KzSqWFNbIazeYD7G7JhxRjLL3GYA130_provenance.
- NP1041596.RACN4U6hZ9r5N_DC1KzSqWFNbIazeYD7G7JhxRjLL3GYA130_assertion SIO_000772 23297359 NP1041596.RACN4U6hZ9r5N_DC1KzSqWFNbIazeYD7G7JhxRjLL3GYA130_provenance.
- NP1041596.RACN4U6hZ9r5N_DC1KzSqWFNbIazeYD7G7JhxRjLL3GYA130_assertion evidence source_evidence_literature NP1041596.RACN4U6hZ9r5N_DC1KzSqWFNbIazeYD7G7JhxRjLL3GYA130_provenance.
- NP1041596.RACN4U6hZ9r5N_DC1KzSqWFNbIazeYD7G7JhxRjLL3GYA130_assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1041596.RACN4U6hZ9r5N_DC1KzSqWFNbIazeYD7G7JhxRjLL3GYA130_provenance.