Naturally occurring glucokinase mutations at the same amino acid residue cause opposite clinical phenotypes of hypo- and hyperglycaemia

Podobne zapisy

• Discovery of a novel site regulating glucokinase activity following characterization of a new mutation causing hyperinsulinemic hypoglycemia in humans.
  od: Beer, N, i wsp.
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  od: Ding, S, i wsp.
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  od: Osbak, K, i wsp.
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