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Q28198461-347443F5-EF7D-438F-A4CD-76917192B653
Q28198461-347443F5-EF7D-438F-A4CD-76917192B653
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28198461-347443F5-EF7D-438F-A4CD-76917192B653
A novel deafness/dystonia peptide gene mutation that causes dystonia in female carriers of Mohr-Tranebjaerg syndrome
P2860
Q28198461-347443F5-EF7D-438F-A4CD-76917192B653
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28198461-347443F5-EF7D-438F-A4CD-76917192B653
rank
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type
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Statement
wasDerivedFrom
2974e7c3e43f334489cb9f16acb5012a0adfd624
P2860
The human family of Deafness/Dystonia peptide (DDP) related mitochondrial import proteins