Associated Papers
A novel glucokinase deletion (p.Lys32del) and five previously described mutations co-segregate with the phenotype of mild familial hyperglycaemia (MODY2) in Brazilian families.
Giuffrida FM et al.
Diabetes Research and Clinical Practice, 2013
Clinical follow-up of two Brazilian subjects with glucokinase-MODY (MODY2) with description of a novel mutation.
DellaManna T et al.
Arquivos Brasileiros De Endocrinologia E Metabologia, 2012
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