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Novel glucokinase gene mutation in the first Macedonian family tested for MODY

Publikace na 2. lékařská fakulta |
2017

Tento text není v aktuálním jazyce dostupný. Zobrazuje se verze "en".Abstrakt

We present a boy with mild hyperglycemia detected during an upper respiratory infection. Novel splicing mutation in the intron 1 of the GCK gene (c.45+1G>A) was detected, and was subsequently confirmed in his father.

This is the first case of genetically confirmed Macedonian family with MODY.