A hemochromatosis-causing mutation C282Y is a risk factor for proliferative diabetic retinopathy in Caucasians with type 2 diabetes
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概要
- 論文の詳細を見る
- Springer-Verlag Tokyoの論文
- 2003-12-01
著者
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Petrovic Daniel
Institute Of Histology And Embryology Medical Faculty University Of Ljubljana
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PETROVIC Mojca
Eye Clinic, University Medical Centre Ljubljana
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HAWLINA Marko
Eye Clinic, University Medical Centre Ljubljana
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PETERLIN Borut
Division of Medical Genetics,Department of Obstetrics and Gynecology,University Medical Centre Ljubl
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GLOBOCNIK PETROVIC
Eye Clinic, University Medical Centre, Ljubljana, Slovenia
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MAKUC Jana
Division of Medical Genetics, Department of Obstetrics and Gynecology, University Medical Centre
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Hawlina Marko
Eye Clinic University Medical Centre Ljubljana
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Peterlin Borut
Division Of Medical Genetics Department Of Obstetrics And Gynaecology University Medical Centre Ljub
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Globocnik Petrovic
Eye Clinic University Medical Centre Ljubljana Slovenia
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Makuc Jana
Division Of Medical Genetics Department Of Obstetrics And Gynecology University Medical Centre
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Peterlin Borut
Division Of Medical Genetics Department Of Obstetrics And Gynecology University Medical Centre Ljubl
関連論文
- Bg/II gene polymorphism of the α2β1 integrin gene is a risk factor for diabetic retinopathy in Caucasians with type 2 diabetes
- A hemochromatosis-causing mutation C282Y is a risk factor for proliferative diabetic retinopathy in Caucasians with type 2 diabetes
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