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Q35629933-D00AB990-BD22-4587-A599-CA2FA5A2C2A1
Q35629933-D00AB990-BD22-4587-A599-CA2FA5A2C2A1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35629933-D00AB990-BD22-4587-A599-CA2FA5A2C2A1
A novel recessive Nefl mutation causes a severe, early-onset axonal neuropathy.
P2860
Q35629933-D00AB990-BD22-4587-A599-CA2FA5A2C2A1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35629933-D00AB990-BD22-4587-A599-CA2FA5A2C2A1
rank
NormalRank
type
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Statement
wasDerivedFrom
eeb7b6da33b2b0300d9a23df43330c8c50db059b
P2860
Charcot-Marie-Tooth disease type 2E, a disorder of the cytoskeleton