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Q33765993-8FBDD21C-4E02-44B6-93B6-4894D0BBE4DE
Q33765993-8FBDD21C-4E02-44B6-93B6-4894D0BBE4DE
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Statement
http://www.wikidata.org/entity/statement/Q33765993-8FBDD21C-4E02-44B6-93B6-4894D0BBE4DE
The role of CTLA-4 exon-1 49 A/G polymorphism and soluble CTLA-4 protein level in egyptian patients with Behçet's disease.
P2860
Q33765993-8FBDD21C-4E02-44B6-93B6-4894D0BBE4DE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33765993-8FBDD21C-4E02-44B6-93B6-4894D0BBE4DE
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Statement
wasDerivedFrom
98e5ab4fbd6ea353b33f86b5720b81ba381f6588
P2860
CTLA-4 gene polymorphism at position 49 in exon 1 reduces the inhibitory function of CTLA-4 and contributes to the pathogenesis of Graves' disease.