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Q36659362-F58D9DCD-4BDF-4777-A592-D63332BDD3F8
Q36659362-F58D9DCD-4BDF-4777-A592-D63332BDD3F8
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Statement
http://www.wikidata.org/entity/statement/Q36659362-F58D9DCD-4BDF-4777-A592-D63332BDD3F8
New NBIA subtype: genetic, clinical, pathologic, and radiographic features of MPAN.
P2860
Q36659362-F58D9DCD-4BDF-4777-A592-D63332BDD3F8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36659362-F58D9DCD-4BDF-4777-A592-D63332BDD3F8
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wasDerivedFrom
6239c7dcfc4c36d38f9d3a146ec5defaef279bd3
P2860
Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation.