French Group of Wolfram Syndrome[Corporate Author] - Search Results

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Identification of novel mutations in WFS1 and genotype-phenotype correlation in Wolfram syndrome.

Cano A, Rouzier C, Monnot S, Chabrol B, Conrath J, Lecomte P, Delobel B, Boileau P, Valero R, Procaccio V, Paquis-Flucklinger V; French Group of Wolfram Syndrome; Vialettes B. Cano A, et al. Am J Med Genet A. 2007 Jul 15;143A(14):1605-12. doi: 10.1002/ajmg.a.31809. Am J Med Genet A. 2007. PMID: 17568405

Microvascular diabetes complications in Wolfram syndrome (diabetes insipidus, diabetes mellitus, optic atrophy, and deafness [DIDMOAD]): an age- and duration-matched comparison with common type 1 diabetes.

Cano A, Molines L, Valéro R, Simonin G, Paquis-Flucklinger V, Vialettes B; French Group of Wolfram Syndrome. Cano A, et al. Diabetes Care. 2007 Sep;30(9):2327-30. doi: 10.2337/dc07-0380. Epub 2007 May 29. Diabetes Care. 2007. PMID: 17536072

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