Prevalence of Maturity-Onset Diabetes of the Young Mutations in Brazilian Families With Autosomal- Dominant Early-Onset Type 2 Diabetes
Author:
Affiliation:
1. Department of Internal Medicine–Endocrinology, Federal University of São Paulo (UNIFESP), São Paulo, Brazil
2. INSERM Unité 342, Paris, France
3. Fondation Jean-Dausset–CEPH, Paris, France
Publisher
American Diabetes Association
Subject
Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine
Link
https://diabetesjournals.org/care/article-pdf/24/4/786/587523/786.pdf
Reference7 articles.
1. Chèvre JC, Hani EH, Boutin P, Vaxillaire M, Blanché H, Vionnet N, Pardini VC, Timsit J, Larger E, Charpentier G, Beckers D, Maes M, Bellanné-Chantelot C, Velho G, Froguel P: Mutation screening in 18 Caucasian families suggests the existence of other MODY genes. Diabetologia 41:1017–1023, 1998
2. Hattersley AT: Maturity onset diabetes of the young: clinical heterogeneity explained by genetic heterogeneity. Diabet Med 15:15–24, 1998
3. Lindner TH, Cockburn BN, Bell GI: Molecular genetics of MODY in Germany. Diabetologia 42:121–123, 1999
4. Lehto M, Wipemo C, Ivarsson SA, Lindgren C, Lipsanen-Nyman M, Weng J, Wibell L, Widen E, Tuomi T, Groop L: High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes. Diabetologia 42:1131–1137, 1999
5. Macfarlane WM, Frayling TM, Ellard S, Evans JC, Allen LIS, Bulman MP, Ayres S, Shepherd M, Clark P, Milward A, Demaine A, Wilkin T, Docherty K, Hattersley AT: Missense mutations in the insulin promoter factor-1 gene predispose to type 2 diabetes. J Clin Invest 104:R33–R39, 1999
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