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- NP865459.RASW3zNVGfanWF45md3EUEUn5iVWLfqAJ4gmkPgEPdoqg130_assertion type Assertion NP865459.RASW3zNVGfanWF45md3EUEUn5iVWLfqAJ4gmkPgEPdoqg130_head.
- NP865459.RASW3zNVGfanWF45md3EUEUn5iVWLfqAJ4gmkPgEPdoqg130_assertion wasGeneratedBy ECO_0000203 NP865459.RASW3zNVGfanWF45md3EUEUn5iVWLfqAJ4gmkPgEPdoqg130_provenance.
- NP865459.RASW3zNVGfanWF45md3EUEUn5iVWLfqAJ4gmkPgEPdoqg130_assertion wasDerivedFrom befree-2016 NP865459.RASW3zNVGfanWF45md3EUEUn5iVWLfqAJ4gmkPgEPdoqg130_provenance.
- NP865459.RASW3zNVGfanWF45md3EUEUn5iVWLfqAJ4gmkPgEPdoqg130_assertion SIO_000772 21236492 NP865459.RASW3zNVGfanWF45md3EUEUn5iVWLfqAJ4gmkPgEPdoqg130_provenance.
- NP865459.RASW3zNVGfanWF45md3EUEUn5iVWLfqAJ4gmkPgEPdoqg130_assertion evidence source_evidence_literature NP865459.RASW3zNVGfanWF45md3EUEUn5iVWLfqAJ4gmkPgEPdoqg130_provenance.
- NP865459.RASW3zNVGfanWF45md3EUEUn5iVWLfqAJ4gmkPgEPdoqg130_assertion description "[A novel mutation of LAMB2 in a multigenerational mennonite family reveals a new phenotypic variant of Pierson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865459.RASW3zNVGfanWF45md3EUEUn5iVWLfqAJ4gmkPgEPdoqg130_provenance.