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Q36194437-422DA97F-CCD3-41FA-AF58-BA2BD6CABF19
Q36194437-422DA97F-CCD3-41FA-AF58-BA2BD6CABF19
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http://www.wikidata.org/entity/statement/Q36194437-422DA97F-CCD3-41FA-AF58-BA2BD6CABF19
Novel homozygous missense mutation in GAN associated with Charcot-Marie-Tooth disease type 2 in a large consanguineous family from Israel.
P2860
Q36194437-422DA97F-CCD3-41FA-AF58-BA2BD6CABF19
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36194437-422DA97F-CCD3-41FA-AF58-BA2BD6CABF19
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wasDerivedFrom
76621ebd6c99598a8beb5084abe2d4802ed0111a
P2860
The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy