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- NP233356.RAgnqnpAZrse6M5RycVOCFFFopQYn5xY6egDr7F-6AR0Q130_assertion type Assertion NP233356.RAgnqnpAZrse6M5RycVOCFFFopQYn5xY6egDr7F-6AR0Q130_head.
- NP233356.RAgnqnpAZrse6M5RycVOCFFFopQYn5xY6egDr7F-6AR0Q130_assertion description "[Mutations in KVLQT1 and KCNE1 also cause the Jervell and Lange-Nielsen syndrome, a form of LQTS associated with deafness, a phenotypic abnormality inherited in an autosomal recessive fashion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP233356.RAgnqnpAZrse6M5RycVOCFFFopQYn5xY6egDr7F-6AR0Q130_provenance.
- NP233356.RAgnqnpAZrse6M5RycVOCFFFopQYn5xY6egDr7F-6AR0Q130_assertion evidence source_evidence_literature NP233356.RAgnqnpAZrse6M5RycVOCFFFopQYn5xY6egDr7F-6AR0Q130_provenance.
- NP233356.RAgnqnpAZrse6M5RycVOCFFFopQYn5xY6egDr7F-6AR0Q130_assertion SIO_000772 10973849 NP233356.RAgnqnpAZrse6M5RycVOCFFFopQYn5xY6egDr7F-6AR0Q130_provenance.
- NP233356.RAgnqnpAZrse6M5RycVOCFFFopQYn5xY6egDr7F-6AR0Q130_assertion wasDerivedFrom befree-20140225 NP233356.RAgnqnpAZrse6M5RycVOCFFFopQYn5xY6egDr7F-6AR0Q130_provenance.
- NP233356.RAgnqnpAZrse6M5RycVOCFFFopQYn5xY6egDr7F-6AR0Q130_assertion wasGeneratedBy ECO_0000203 NP233356.RAgnqnpAZrse6M5RycVOCFFFopQYn5xY6egDr7F-6AR0Q130_provenance.