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Q48328429-7E0A22EA-CDBC-4C90-9918-BA7042CE6898
Q48328429-7E0A22EA-CDBC-4C90-9918-BA7042CE6898
BestRank
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http://www.wikidata.org/entity/statement/Q48328429-7E0A22EA-CDBC-4C90-9918-BA7042CE6898
A homozygous splice variant in AP4S1 mimicking neurodegeneration with brain iron accumulation.
P2860
Q48328429-7E0A22EA-CDBC-4C90-9918-BA7042CE6898
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48328429-7E0A22EA-CDBC-4C90-9918-BA7042CE6898
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wasDerivedFrom
b55c64a1443f1a9a7e4df572de2407a7eccf7bee
P2860
Mutation in the AP4M1 gene provides a model for neuroaxonal injury in cerebral palsy