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Q35643742-4CB89BBF-FD0D-4307-B25A-FAE86CB17FD3
Q35643742-4CB89BBF-FD0D-4307-B25A-FAE86CB17FD3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35643742-4CB89BBF-FD0D-4307-B25A-FAE86CB17FD3
A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies.
P2860
Q35643742-4CB89BBF-FD0D-4307-B25A-FAE86CB17FD3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35643742-4CB89BBF-FD0D-4307-B25A-FAE86CB17FD3
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type
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wasDerivedFrom
01f4efdf1e28c31f2697213a23393ebfc367b443
P2860
Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A.