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Q36082741-8EF17F22-4028-4368-91D7-D4F15CA8B7B1
Q36082741-8EF17F22-4028-4368-91D7-D4F15CA8B7B1
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http://www.wikidata.org/entity/statement/Q36082741-8EF17F22-4028-4368-91D7-D4F15CA8B7B1
Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3.
P2860
Q36082741-8EF17F22-4028-4368-91D7-D4F15CA8B7B1
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http://www.wikidata.org/entity/statement/Q36082741-8EF17F22-4028-4368-91D7-D4F15CA8B7B1
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wasDerivedFrom
64bd248cc4fe54b7c7a35de287905b4328a7598c
P2860
Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A.