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Lehto M, Tuomi T, Mahtani MM, Widén E, Forsblom C, Sarelin L, Gullström, Isomaa B, Lehtovirta M, Hyrkkö A, Kanninen T, Orho M, Manley S, Turner RC, Brettin T, Kirby A, Thomas J, Duyk G, Lander E, Taskinen M-R, Groop L: Characterization of the MODY3 phenotype: early-onset diabetes caused by an insulin secretion defect. J Clin Invest 99:582-591, 1997
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Isomaa, B.8
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Brettin, T.15
Kirby, A.16
Thomas, J.17
Duyk, G.18
Lander, E.19
Taskinen, M.-R.20
Groop, L.21
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Genetic variation in the hepatocyte nuclear factor- 1α gene in Danish Caucasians with late-onset NIDDM
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Urhammer SA, Rasmussen SK, Kaisaki PJ, Oda N, Yamagata K, Møller AM, Fridberg M, Hansen L, Hansen T, Bell GI, Pedersen O: Genetic variation in the hepatocyte nuclear factor-1α gene in Danish Caucasians with late-onset NIDDM. Diabetologia 40:473-475, 1997
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Urhammer, S.A.1
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Hansen, T.9
Bell, G.I.10
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Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families
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Velho G, Blanché H, Vaxillaire M, Bellanné-Chantelot, Pardini VC, Timsit J, Passa P, Deschamps I, Robert J-J, Weber IT, Marotta D, Pilkis SJ, Lipkind GM, Bell GI, Froguel P: Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families. Diabetologia 40:217-224, 1997
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Velho, G.1
Blanché, H.2
Vaxillaire, M.3
Bellanné-Chantelot4
Pardini, V.C.5
Timsit, J.6
Passa, P.7
Deschamps, I.8
Robert, J.-J.9
Weber, I.T.10
Marotta, D.11
Pilkis, S.J.12
Lipkind, G.M.13
Bell, G.I.14
Froguel, P.15
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