Mutations in the SLC30A8 gene are not a major cause of MODY or other forms of early-onset, autosomal dominant type 2 diabetes

By Borowiec M.   Thompson R.   Powers C.   Xu R.   Dickey T.   Doria A.  

Diabetologia, Vol. 50, Iss. 10, 2007-10 ,pp. : 2224-2226

Springer Publishing Company

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The common SLC30A8 Arg325Trp variant is associated with reduced first-phase insulin release in 846 non-diabetic offspring of type 2 diabetes patients—the EUGENE2 study

By Boesgaard T.   Žilinskaitė J.   Vänttinen M.   Laakso M.   Jansson P.-A.   Hammarstedt A.   Smith U.   Stefan N.   Fritsche A.   Häring H.   Hribal M.   Sesti G.   Zobel D.   Pedersen O.   Hansen T.  

Diabetologia, Vol. 51, Iss. 5, 2008-05 ,pp. : 816-820

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The ATP-Binding Cassette Transporter Subfamily A Member 1 (ABC-A1) and Type 2 Diabetes: An Association Beyond HDL Cholesterol

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Current Diabetes Reviews, Vol. 3, Iss. 4, 2007-11 ,pp. : 264-267

Bentham Science Publishers

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Connecting the Dots: Molecular and Epigenetic Mechanisms in Type 2 Diabetes

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Current Diabetes Reviews, Vol. 6, Iss. 4, 2010-07 ,pp. : 255-265

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Genetic etiology of type 2 diabetes mellitus: a review

By Kommoju Uma  

International Journal of Diabetes in Developing Countries, Vol. 31, Iss. 2, 2011-04 ,pp. : 51-64

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