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Q30501423-2DB15088-29FA-4D20-B649-6F8CC65EA4D3
Q30501423-2DB15088-29FA-4D20-B649-6F8CC65EA4D3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30501423-2DB15088-29FA-4D20-B649-6F8CC65EA4D3
A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafness.
P2860
Q30501423-2DB15088-29FA-4D20-B649-6F8CC65EA4D3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30501423-2DB15088-29FA-4D20-B649-6F8CC65EA4D3
rank
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wasDerivedFrom
50382e6ab8344d4010a655915e2932d7a874c072
P2860
Slowing of central conduction in X-linked Charcot-Marie-Tooth neuropathy shown by brain stem auditory evoked responses.