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Q24315627-73A14D19-9753-45A1-A827-B6FFE54B9CF7
Q24315627-73A14D19-9753-45A1-A827-B6FFE54B9CF7
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http://www.wikidata.org/entity/statement/Q24315627-73A14D19-9753-45A1-A827-B6FFE54B9CF7
Exome sequence reveals mutations in CoA synthase as a cause of neurodegeneration with brain iron accumulation
P2860
Q24315627-73A14D19-9753-45A1-A827-B6FFE54B9CF7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24315627-73A14D19-9753-45A1-A827-B6FFE54B9CF7
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wasDerivedFrom
e2896214dc97086300ceb47f5cd0e395f057495b
P2860
Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation.