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Q51076518-6D69D1F8-A481-4872-91A2-8C7C1BE821D8
Q51076518-6D69D1F8-A481-4872-91A2-8C7C1BE821D8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51076518-6D69D1F8-A481-4872-91A2-8C7C1BE821D8
The Phe932Ile mutation in KCNT1 channels associated with severe epilepsy, delayed myelination and leukoencephalopathy produces a loss-of-function channel phenotype.
P407
Q51076518-6D69D1F8-A481-4872-91A2-8C7C1BE821D8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51076518-6D69D1F8-A481-4872-91A2-8C7C1BE821D8
rank
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type
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P407
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