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Q28198461-8CA2F901-E0A3-4485-973B-0D288E87AF76
Q28198461-8CA2F901-E0A3-4485-973B-0D288E87AF76
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28198461-8CA2F901-E0A3-4485-973B-0D288E87AF76
A novel deafness/dystonia peptide gene mutation that causes dystonia in female carriers of Mohr-Tranebjaerg syndrome
P2860
Q28198461-8CA2F901-E0A3-4485-973B-0D288E87AF76
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28198461-8CA2F901-E0A3-4485-973B-0D288E87AF76
rank
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type
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Statement
wasDerivedFrom
2974e7c3e43f334489cb9f16acb5012a0adfd624
P2860
A de novo missense mutation in a critical domain of the X-linked DDP gene causes the typical deafness-dystonia-optic atrophy syndrome