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- NP636681.RAVnDWxntWloqFHkEL1ohMgEe0AQjO6-cztso35xZvZhI130_assertion type Assertion NP636681.RAVnDWxntWloqFHkEL1ohMgEe0AQjO6-cztso35xZvZhI130_head.
- NP636681.RAVnDWxntWloqFHkEL1ohMgEe0AQjO6-cztso35xZvZhI130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636681.RAVnDWxntWloqFHkEL1ohMgEe0AQjO6-cztso35xZvZhI130_provenance.
- NP636681.RAVnDWxntWloqFHkEL1ohMgEe0AQjO6-cztso35xZvZhI130_assertion evidence source_evidence_literature NP636681.RAVnDWxntWloqFHkEL1ohMgEe0AQjO6-cztso35xZvZhI130_provenance.
- NP636681.RAVnDWxntWloqFHkEL1ohMgEe0AQjO6-cztso35xZvZhI130_assertion SIO_000772 17952667 NP636681.RAVnDWxntWloqFHkEL1ohMgEe0AQjO6-cztso35xZvZhI130_provenance.
- NP636681.RAVnDWxntWloqFHkEL1ohMgEe0AQjO6-cztso35xZvZhI130_assertion wasDerivedFrom befree-2016 NP636681.RAVnDWxntWloqFHkEL1ohMgEe0AQjO6-cztso35xZvZhI130_provenance.
- NP636681.RAVnDWxntWloqFHkEL1ohMgEe0AQjO6-cztso35xZvZhI130_assertion wasGeneratedBy ECO_0000203 NP636681.RAVnDWxntWloqFHkEL1ohMgEe0AQjO6-cztso35xZvZhI130_provenance.