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Q52421616-6724958B-E118-4A7D-87A4-8FC5527A373B
Q52421616-6724958B-E118-4A7D-87A4-8FC5527A373B
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http://www.wikidata.org/entity/statement/Q52421616-6724958B-E118-4A7D-87A4-8FC5527A373B
Clinical and genetic characterization of AP4B1-associated SPG47.
P2860
Q52421616-6724958B-E118-4A7D-87A4-8FC5527A373B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52421616-6724958B-E118-4A7D-87A4-8FC5527A373B
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5f1d12aa987aad07139a21d2e95e19fb02d43b59
P2860
Mutation in the AP4M1 gene provides a model for neuroaxonal injury in cerebral palsy