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- NP665378.RAz3RJn05z9tzD6a-YgP1WUjfPPI_7M-2U2mjTceu1t74130_assertion type Assertion NP665378.RAz3RJn05z9tzD6a-YgP1WUjfPPI_7M-2U2mjTceu1t74130_head.
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- NP665378.RAz3RJn05z9tzD6a-YgP1WUjfPPI_7M-2U2mjTceu1t74130_assertion wasDerivedFrom befree-20140225 NP665378.RAz3RJn05z9tzD6a-YgP1WUjfPPI_7M-2U2mjTceu1t74130_provenance.
- NP665378.RAz3RJn05z9tzD6a-YgP1WUjfPPI_7M-2U2mjTceu1t74130_assertion SIO_000772 15580558 NP665378.RAz3RJn05z9tzD6a-YgP1WUjfPPI_7M-2U2mjTceu1t74130_provenance.
- NP665378.RAz3RJn05z9tzD6a-YgP1WUjfPPI_7M-2U2mjTceu1t74130_assertion evidence source_evidence_literature NP665378.RAz3RJn05z9tzD6a-YgP1WUjfPPI_7M-2U2mjTceu1t74130_provenance.
- NP665378.RAz3RJn05z9tzD6a-YgP1WUjfPPI_7M-2U2mjTceu1t74130_assertion description "[We conclude that KCNJ11 mutations are a common cause of PNDM either in isolation or associated with developmental delay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665378.RAz3RJn05z9tzD6a-YgP1WUjfPPI_7M-2U2mjTceu1t74130_provenance.