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High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes

Markku Lehto, C. Wipemo, S A Ivarsson, Cecilia M. Lindgren, Marita Lipsanen‐Nyman, Jianping Weng, L Wibell, Elisabeth Widén, Leif Groop

Diabetologia · 1999 · 137 citations · 13 references

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13

Mutations in the hepatocyte nuclear factor-1α gene in maturity-onset diabetes of the young (MODY3)

Kazuya Yamagata, Naohisa Oda, Pamela J. Kaisaki et al. · Nature · 1996 · 1.6K citations · Full text

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Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

J. M. W. van den Ouweland, H.H.P.J. Lemkes, W. Ruitenbeek et al. · Nature Genetics · 1992 · 1.1K citations

, , +15

Clinical and genetic characteristics of type 2 diabetes with and without GAD antibodies.

Annelie Carlsson, H Li, Bo Isomaa et al. · Diabetes · 1999 · 506 citations

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Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defect.

Markku Lehto, Melanie M. Mahtani, Elisabeth Widén et al. · Journal of Clinical Investigation · 1997 · 199 citations · Full text

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Mutation screening in 18 Caucasian families suggest the existence of other MODY genes

Jean-Claude Chèvre, El Habib Hani, Philippe Boutin et al. · Diabetologia · 1998 · 142 citations · Full text

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