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- NP390684.RAyXDg-VysX-vAHOUQkEF05IFrrE-nGbqh127OTlr0G80130_assertion type Assertion NP390684.RAyXDg-VysX-vAHOUQkEF05IFrrE-nGbqh127OTlr0G80130_head.
- NP390684.RAyXDg-VysX-vAHOUQkEF05IFrrE-nGbqh127OTlr0G80130_assertion wasGeneratedBy ECO_0000203 NP390684.RAyXDg-VysX-vAHOUQkEF05IFrrE-nGbqh127OTlr0G80130_provenance.
- NP390684.RAyXDg-VysX-vAHOUQkEF05IFrrE-nGbqh127OTlr0G80130_assertion wasDerivedFrom befree-20140225 NP390684.RAyXDg-VysX-vAHOUQkEF05IFrrE-nGbqh127OTlr0G80130_provenance.
- NP390684.RAyXDg-VysX-vAHOUQkEF05IFrrE-nGbqh127OTlr0G80130_assertion SIO_000772 20130826 NP390684.RAyXDg-VysX-vAHOUQkEF05IFrrE-nGbqh127OTlr0G80130_provenance.
- NP390684.RAyXDg-VysX-vAHOUQkEF05IFrrE-nGbqh127OTlr0G80130_assertion evidence source_evidence_literature NP390684.RAyXDg-VysX-vAHOUQkEF05IFrrE-nGbqh127OTlr0G80130_provenance.
- NP390684.RAyXDg-VysX-vAHOUQkEF05IFrrE-nGbqh127OTlr0G80130_assertion description "[Mutations in SOX10 are associated with several neurocristopathies such as Waardenburg syndrome type IV (WS4), a congenital disorder characterized by the association of hearing loss, pigmentary abnormalities, and absence of ganglion cells in the myenteric and submucosal plexus of the gastrointestinal tract, also known as aganglionic megacolon or Hirschsprung disease (HSCR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390684.RAyXDg-VysX-vAHOUQkEF05IFrrE-nGbqh127OTlr0G80130_provenance.