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Q36507186-5F6885BA-A350-47C4-822E-F6A0310E8390
Q36507186-5F6885BA-A350-47C4-822E-F6A0310E8390
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36507186-5F6885BA-A350-47C4-822E-F6A0310E8390
Molecular diagnostics of Charcot-Marie-Tooth disease and related peripheral neuropathies.
P2860
Q36507186-5F6885BA-A350-47C4-822E-F6A0310E8390
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36507186-5F6885BA-A350-47C4-822E-F6A0310E8390
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wasDerivedFrom
759ecfb63943f6b2816d7a89f164d0ea2b1548dd
P2860
A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafness.