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Q53439745-473181E1-545E-40E0-96DB-58D354F5C80B
Q53439745-473181E1-545E-40E0-96DB-58D354F5C80B
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http://www.wikidata.org/entity/statement/Q53439745-473181E1-545E-40E0-96DB-58D354F5C80B
X-linked dominant Charcot-Marie-Tooth disease with connexin 32 (Cx32) mutations in Koreans.
P2860
Q53439745-473181E1-545E-40E0-96DB-58D354F5C80B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53439745-473181E1-545E-40E0-96DB-58D354F5C80B
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wasDerivedFrom
648c9f764a000bd671cfb6253093130fb7cf893a
P2860
Mutation analysis of the PMP22, MPZ, EGR2, LITAF, and GJB1 genes in Korean patients with Charcot-Marie-Tooth neuropathy type 1.