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Q30981903-86ADFF47-B74A-40F4-B8C1-0C5D63100215
Q30981903-86ADFF47-B74A-40F4-B8C1-0C5D63100215
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30981903-86ADFF47-B74A-40F4-B8C1-0C5D63100215
Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia.
P2860
Q30981903-86ADFF47-B74A-40F4-B8C1-0C5D63100215
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30981903-86ADFF47-B74A-40F4-B8C1-0C5D63100215
rank
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type
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Statement
wasDerivedFrom
16e1f5a3186d6eeaace3de1dc972d9c07f3c29fb
P2860
Epilepsy: old syndromes, new genes.