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MODY Syndrome / 대한소아내분비학회지
Journal of Korean Society of Pediatric Endocrinology ; : 1-6, 2010.
Article in Korean | WPRIM | ID: wpr-19831
ABSTRACT
Maturity-onset diabetes of the young (MODY) is a heterogenous form of diabetes characterized by the early onset of diabetes, autosomal dominant inheritance, and impaired insulin secretion. MODY is mostly caused by mutations of the hepatocyte nuclear factor 1-alpha (HNF1-alpha) and glucokinase genes in Caucasians. However most Korean, Japanese, and Chinese patients with MODY do not express known MODY genes. The cause of MODY in Asians has not yet been elucidated clearly. This review focuses on studies on Asian patients with MODY.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Wills / Asian People / Diabetes Mellitus, Type 2 / Hepatocyte Nuclear Factor 1-alpha / Glucokinase / Insulin Limits: Humans Language: Korean Journal: Journal of Korean Society of Pediatric Endocrinology Year: 2010 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Wills / Asian People / Diabetes Mellitus, Type 2 / Hepatocyte Nuclear Factor 1-alpha / Glucokinase / Insulin Limits: Humans Language: Korean Journal: Journal of Korean Society of Pediatric Endocrinology Year: 2010 Type: Article