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Q38275252-2A22EA75-1FFB-43F6-86FB-E1BF108A7DFC
Q38275252-2A22EA75-1FFB-43F6-86FB-E1BF108A7DFC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38275252-2A22EA75-1FFB-43F6-86FB-E1BF108A7DFC
The expanding spectrum of neurological phenotypes in children with ATP1A3 mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and beyond.
P2860
Q38275252-2A22EA75-1FFB-43F6-86FB-E1BF108A7DFC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38275252-2A22EA75-1FFB-43F6-86FB-E1BF108A7DFC
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type
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wasDerivedFrom
8a41c62cd8b3079eb4c9c03cf8cda8ee0d5ac352
P2860
Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures