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[In humans, a copy number loss of 22q11.2, a region harboring the VPREB1 gene, has been suggested to be associated with several immunologic disorders, but there has been no study on the copy number variation (CNV) of the VPREB1 and its potential association with RA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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