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Q37576096-4DC685C7-0B96-49E5-BF3E-1B615A7A7F95
Q37576096-4DC685C7-0B96-49E5-BF3E-1B615A7A7F95
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37576096-4DC685C7-0B96-49E5-BF3E-1B615A7A7F95
Loss of Coupling Distinguishes GJB1 Mutations Associated with CNS Manifestations of CMT1X from Those Without CNS Manifestations.
P2860
Q37576096-4DC685C7-0B96-49E5-BF3E-1B615A7A7F95
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37576096-4DC685C7-0B96-49E5-BF3E-1B615A7A7F95
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Statement
wasDerivedFrom
7f2921a3e09d00d4ade206c2f7ee22ab4a744a7d
P2860
The central nervous system phenotype of X-linked Charcot-Marie-Tooth disease: a transient disorder of children and young adults.