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Whole-exome sequencing in a Japanese family with highly aggregated diabetes identifies a candidate susceptibility mutation in ADAMTSL3

in Brighter - diabetes in family

Whole-exome sequencing in a Japanese family with highly aggregated diabetes identifies a candidate susceptibility mutation in ADAMTSL3

Source: Medworm

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Diabetes is a disease of dysfunctional glucose regulation. The predominant types are type 1 diabetes (T1D) and type 2 diabetes (T2D). T1D is an organ-specific autoimmune disease that results from the progressive loss of insulin-producing β-cells in the pancreas. T1D represents a polygenic disorder [1].

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