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- NP324660.RAAOZirkkW6J7f2c4to6RDUrTQhuoreu377Tif-wDrGWg130_assertion type Assertion NP324660.RAAOZirkkW6J7f2c4to6RDUrTQhuoreu377Tif-wDrGWg130_head.
- NP324660.RAAOZirkkW6J7f2c4to6RDUrTQhuoreu377Tif-wDrGWg130_assertion description "[Mutations in the X-chromosomal gene (L1CAM) for cell adhesion molecule L1 are associated with a heterogeneous group of conditions that include agenesis of the corpus callosum, hydrocephalus, spastic paraplegia, adducted thumbs and mental retardation (L1-spectrum disease, CRASH or MASA syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324660.RAAOZirkkW6J7f2c4to6RDUrTQhuoreu377Tif-wDrGWg130_provenance.
- NP324660.RAAOZirkkW6J7f2c4to6RDUrTQhuoreu377Tif-wDrGWg130_assertion evidence source_evidence_literature NP324660.RAAOZirkkW6J7f2c4to6RDUrTQhuoreu377Tif-wDrGWg130_provenance.
- NP324660.RAAOZirkkW6J7f2c4to6RDUrTQhuoreu377Tif-wDrGWg130_assertion SIO_000772 17294222 NP324660.RAAOZirkkW6J7f2c4to6RDUrTQhuoreu377Tif-wDrGWg130_provenance.
- NP324660.RAAOZirkkW6J7f2c4to6RDUrTQhuoreu377Tif-wDrGWg130_assertion wasDerivedFrom befree-20140225 NP324660.RAAOZirkkW6J7f2c4to6RDUrTQhuoreu377Tif-wDrGWg130_provenance.
- NP324660.RAAOZirkkW6J7f2c4to6RDUrTQhuoreu377Tif-wDrGWg130_assertion wasGeneratedBy ECO_0000203 NP324660.RAAOZirkkW6J7f2c4to6RDUrTQhuoreu377Tif-wDrGWg130_provenance.