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Q52137131-97ADAF1F-E613-48A4-B0FD-F443F675C12B
Q52137131-97ADAF1F-E613-48A4-B0FD-F443F675C12B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52137131-97ADAF1F-E613-48A4-B0FD-F443F675C12B
A novel de novo dominant negative mutation in DNM1L impairs mitochondrial fission and presents as childhood epileptic encephalopathy.
P478
Q52137131-97ADAF1F-E613-48A4-B0FD-F443F675C12B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52137131-97ADAF1F-E613-48A4-B0FD-F443F675C12B
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
0abee08e8308e9e2a974d76ad36c61ebe5dfe9cb
P478
170
http://www.w3.org/2001/XMLSchema#string