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MODY2 in Asia: analysis of GCK mutations and clinical characteristics
Aims: Heterozygous inactivating mutations in the GCK gene cause the familial, mild fasting hyperglycaemia named MODY2. Many patients with MODY2 in Asia have delayed timely treatment because they did not receive the correct diagn osis. This study aims to analyze the clinical characteristics and GCK m...
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| Asıl Yazarlar: | , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Bioscientifica
2020-06-01
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| Seri Bilgileri: | Endocrine Connections |
| Konular: | |
| Online Erişim: | https://ec.bioscientifica.com/view/journals/ec/9/5/EC-20-0074.xml |
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