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Q35286584-205294F2-3CEE-4C7F-A0CC-F82BBA53C02B
Q35286584-205294F2-3CEE-4C7F-A0CC-F82BBA53C02B
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Statement
http://www.wikidata.org/entity/statement/Q35286584-205294F2-3CEE-4C7F-A0CC-F82BBA53C02B
Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation.
P2860
Q35286584-205294F2-3CEE-4C7F-A0CC-F82BBA53C02B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35286584-205294F2-3CEE-4C7F-A0CC-F82BBA53C02B
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wasDerivedFrom
b6ababf2d719b87e2b597a51810c210c4ecdbd9d
P2860
Genetic analysis of pathways to Parkinson disease.