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Q38702643-7DBBEEB6-E815-4296-94AF-B8B89EBA86A8
Q38702643-7DBBEEB6-E815-4296-94AF-B8B89EBA86A8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38702643-7DBBEEB6-E815-4296-94AF-B8B89EBA86A8
FOXG1 syndrome: genotype-phenotype association in 83 patients with FOXG1 variants.
P2860
Q38702643-7DBBEEB6-E815-4296-94AF-B8B89EBA86A8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38702643-7DBBEEB6-E815-4296-94AF-B8B89EBA86A8
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Statement
wasDerivedFrom
390f2d9e0cfc95599c2f3a3b94862df405206f2e
P2860
The expanding spectrum of neurological phenotypes in children with ATP1A3 mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and beyond.