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URL: http://fusion.sph.umich.edu/
Proper Citation: FUSION study (RRID:SCR_016580)
Description: Portal to map and identify genetic variants that predispose to type 2 diabetes mellitus (T2D) or are responsible for variability in diabetes-related quantitative traits. Used for analysis of affected-sibling-pair (ASP) families in Finland, and association fine mapping based on these family members and additional T2D cases and controls.
Abbreviations: FUSION
Synonyms: Finland United States Investigation of NIDDM genetics
Resource Type: topical portal, portal, disease-related portal, data or information resource
Keywords: map, identify, genetic, variant, predispose, type II diabetes, mellitus, T2D
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