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Q41643440-74CE26F8-27DD-4D2F-866F-68E0BCB3F1D7
Q41643440-74CE26F8-27DD-4D2F-866F-68E0BCB3F1D7
BestRank
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http://www.wikidata.org/entity/statement/Q41643440-74CE26F8-27DD-4D2F-866F-68E0BCB3F1D7
Nonrecurrent PMP22-RAI1 contiguous gene deletions arise from replication-based mechanisms and result in Smith-Magenis syndrome with evident peripheral neuropathy.
P2860
Q41643440-74CE26F8-27DD-4D2F-866F-68E0BCB3F1D7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41643440-74CE26F8-27DD-4D2F-866F-68E0BCB3F1D7
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Statement
wasDerivedFrom
baf3c1e7a8690f313e390410339e5e72b17c1962
P2860
The phenotype of recurrent 10q22q23 deletions and duplications.