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Q47132491-4BE20DC2-7C13-4D5A-9D3C-D58EEB22E9E7
Q47132491-4BE20DC2-7C13-4D5A-9D3C-D58EEB22E9E7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47132491-4BE20DC2-7C13-4D5A-9D3C-D58EEB22E9E7
ATP1A3 mutations can cause progressive auditory neuropathy: a new gene of auditory synaptopathy.
P2860
Q47132491-4BE20DC2-7C13-4D5A-9D3C-D58EEB22E9E7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47132491-4BE20DC2-7C13-4D5A-9D3C-D58EEB22E9E7
rank
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type
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Statement
wasDerivedFrom
f2065cb26e95260a5e48da06a92e6696ee5f624b
P2860
The expanding spectrum of neurological phenotypes in children with ATP1A3 mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and beyond.