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- NP461157.RAR9CQoqWs1ukEed5RKvlxuCtOviBh6cgdnMLDON1nWI8130_assertion type Assertion NP461157.RAR9CQoqWs1ukEed5RKvlxuCtOviBh6cgdnMLDON1nWI8130_head.
- NP461157.RAR9CQoqWs1ukEed5RKvlxuCtOviBh6cgdnMLDON1nWI8130_assertion wasGeneratedBy ECO_0000203 NP461157.RAR9CQoqWs1ukEed5RKvlxuCtOviBh6cgdnMLDON1nWI8130_provenance.
- NP461157.RAR9CQoqWs1ukEed5RKvlxuCtOviBh6cgdnMLDON1nWI8130_assertion wasDerivedFrom befree-2016 NP461157.RAR9CQoqWs1ukEed5RKvlxuCtOviBh6cgdnMLDON1nWI8130_provenance.
- NP461157.RAR9CQoqWs1ukEed5RKvlxuCtOviBh6cgdnMLDON1nWI8130_assertion SIO_000772 15383666 NP461157.RAR9CQoqWs1ukEed5RKvlxuCtOviBh6cgdnMLDON1nWI8130_provenance.
- NP461157.RAR9CQoqWs1ukEed5RKvlxuCtOviBh6cgdnMLDON1nWI8130_assertion evidence source_evidence_literature NP461157.RAR9CQoqWs1ukEed5RKvlxuCtOviBh6cgdnMLDON1nWI8130_provenance.
- NP461157.RAR9CQoqWs1ukEed5RKvlxuCtOviBh6cgdnMLDON1nWI8130_assertion description "[Mutations in the hPOMT1 gene are responsible for Walker-Warburg syndrome (WWS), a severe recessive congenital muscular dystrophy associated with defects in neuronal migration that produce complex brain and eye abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP461157.RAR9CQoqWs1ukEed5RKvlxuCtOviBh6cgdnMLDON1nWI8130_provenance.