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https://doi.org/10.1016/j.diabres.2014.08.006
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Cite Publication Date: Aug 12, 2014 | |
 Citations: 10 |
Thirty-two Brazilian families with MODY phenotype were screened for GCK and HNF1A mutations. GCK mutations were found in 8 families, all patients with mild asymptomatic hyperglycaemia; 3 of them are novel: p.Asp365Asn, p.Gly81Asp and p.Val253Leu. Previously described mutations in HNF1A were found in 2 families.
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