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Although guidelines often exclude MODY if autoantibodies are present, the two diagnoses are not mutually exclusive
Chen W, Jiang T, Wang H, Tao S, Lau A, Fang D, et al
Among the primary human classes of this system, GSTM1 and GSTT1 genes exhibit a deletion polymorphism that leads to a lack of active isoforms when in homozygosis, known as the null genotype [9]
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