Three novel mutations in MODY and its phenotype in three different Czech families

Abstract Aims/hypothesis MODY (Maturity Onset Diabetes of the Young) is an autosomal dominant inherited type of diabetes with significant genetic heterogeneity. New mutations causing MODY are still being found. A genetically confirmed diagnosis of MODY allows application of individualized treatment...

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Veröffentlicht in:	Diabetes research and clinical practice 2010-05, Vol.88 (2), p.132-138
Hauptverfasser:	Bazalová, Z, Rypáčková, B, Brož, J, Brunerová, L, Polák, J, Rušavý, Z, Trešlová, L, Anděl, M
Format:	Artikel
Sprache:	eng
Schlagworte:	Czechoslovakia Diabetes Mellitus - drug therapy Diabetes Mellitus - genetics Diet Therapy Endocrinology & Metabolism Family Health GCK Gliclazide - therapeutic use Glucokinase - genetics Hepatocyte Nuclear Factor 1-alpha - genetics Hepatocyte Nuclear Factor 4 - genetics HNF1A Humans Hypoglycemic Agents Insulin - therapeutic use MODY Mutation Novel mutation Pedigree Phenotype Treatment Outcome
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