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Q30501423-3F775DA9-8645-4510-9978-AF4E2CEEAB3F
Q30501423-3F775DA9-8645-4510-9978-AF4E2CEEAB3F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30501423-3F775DA9-8645-4510-9978-AF4E2CEEAB3F
A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafness.
P2860
Q30501423-3F775DA9-8645-4510-9978-AF4E2CEEAB3F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30501423-3F775DA9-8645-4510-9978-AF4E2CEEAB3F
rank
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Statement
wasDerivedFrom
50382e6ab8344d4010a655915e2932d7a874c072
P2860
Characterization of a novel peripheral nervous system myelin protein (PMP-22/SR13)