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Q30501423-63E13D27-387B-49CB-B71F-DDA716C2F8C3
Q30501423-63E13D27-387B-49CB-B71F-DDA716C2F8C3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30501423-63E13D27-387B-49CB-B71F-DDA716C2F8C3
A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafness.
P2093
Q30501423-63E13D27-387B-49CB-B71F-DDA716C2F8C3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30501423-63E13D27-387B-49CB-B71F-DDA716C2F8C3
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
50a8f01efe648359031217639a059ad335a30f7c
P1545
11
http://www.w3.org/2001/XMLSchema#string
P2093
D Gelber
http://www.w3.org/2001/XMLSchema#string