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Q38275252-34725368-62B0-4A3A-B24F-4E39F70451EA
Q38275252-34725368-62B0-4A3A-B24F-4E39F70451EA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38275252-34725368-62B0-4A3A-B24F-4E39F70451EA
The expanding spectrum of neurological phenotypes in children with ATP1A3 mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and beyond.
P2860
Q38275252-34725368-62B0-4A3A-B24F-4E39F70451EA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38275252-34725368-62B0-4A3A-B24F-4E39F70451EA
rank
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Statement
wasDerivedFrom
be83e0ed21d378888781f1cb3e1502ef2fac883d
P2860
Two novel SCN1A mutations identified in families with familial hemiplegic migraine.